<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOph</journal-id><journal-title-group><journal-title>Open Journal of Ophthalmology</journal-title></journal-title-group><issn pub-type="epub">2165-7408</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojoph.2018.84027</article-id><article-id pub-id-type="publisher-id">OJOph-88699</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Natural History and Treatment of Brown’s Syndrome: Long-Term Experience
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pedro</surname><given-names>Filipe Rodrigues</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Raquel</surname><given-names>Seldon</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gabriela</surname><given-names>Varandas</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Maria</surname><given-names>Lourdes Vieira</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Instituto de Oftalmologia Dr. Gama Pinto, Lisbon, Portugal</addr-line></aff><pub-date pub-type="epub"><day>28</day><month>09</month><year>2018</year></pub-date><volume>08</volume><issue>04</issue><fpage>232</fpage><lpage>240</lpage><history><date date-type="received"><day>22,</day>	<month>October</month>	<year>2018</year></date><date date-type="rev-recd"><day>19,</day>	<month>November</month>	<year>2018</year>	</date><date date-type="accepted"><day>23,</day>	<month>November</month>	<year>2018</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Purpose: Brown’s Syndrome (BS) is a restrictive strabismus characterized by a limitation of elevation in adduction. Several etiologies have been described, usually involving the superior oblique muscle. Spontaneous improvement has been reported in several studies, so surgery is reserved for a minority of cases. Our purpose is to review the characteristics, natural history and treatment of this pathology and present the experience of the Instituto de Oftalmologia Dr. Gama Pinto (IOGP). 
  Methods: A consecutive retrospective series of BS patients seen at the Strabismus Department of IOGP between 1983 and 2014 was reviewed. All patients with complete clinical data were included in this study. The epidemiologic characteristics, clinical features, treatment, and clinical progression were reviewed. 
  Results: Thirty-nine cases were selected, with a mean age at first diagnosis of 6.5 years. Of the thirty-nine cases, 6 were iatrogenic and the remainder idiopathic. Thirty-six cases were followed for a mean period of 6.1 years. Surgical intervention for BS was performed in 11 patients, using different approaches. Of these, 9 cases were considered successful. The remaining 25 cases were kept under observation without surgery, of which 17 showed spontaneous improvement and the other 7 remained unchanged. Conclusions: The surgical success rate was 82%, which demonstrates the good efficacy of the surgery despite the complexity and variety of pathophysiological mechanisms of the syndrome. In the patients kept under observation there was spontaneous improvement in 68%, confirming that a conservative approach seems to be adequate in most cases.
 
</p></abstract><kwd-group><kwd>Brown’s Syndrome</kwd><kwd> Extraocular Muscles</kwd><kwd> Strabismus</kwd><kwd> Superior Oblique Muscle</kwd><kwd> Surgery</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Brown’s Syndrome (BS) is a type of restrictive strabismus that presents with a limitation of elevation in adduction and a positive forced duction test [<xref ref-type="bibr" rid="scirp.88699-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref5">5</xref>] . It can be classified into mild, moderate (if a downshoot in adduction is present) and severe forms (if hypotropia in the primary position is present) [<xref ref-type="bibr" rid="scirp.88699-ref6">6</xref>] .</p><p>Binocular function is usually preserved, even in severe cases, via a compensatory anomalous head position [<xref ref-type="bibr" rid="scirp.88699-ref5">5</xref>] . The presence of amblyopia is uncommon, varying between 4% and 25% of the cases, with lack of fusion as the greatest risk factor [<xref ref-type="bibr" rid="scirp.88699-ref7">7</xref>] .</p><p>Brown [<xref ref-type="bibr" rid="scirp.88699-ref8">8</xref>] originally considered that the syndrome was caused by a shortening of the tendon sheath of the superior oblique muscle (SO). However, since then, different etiologies have been found, either based on SO abnormalities [<xref ref-type="bibr" rid="scirp.88699-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref9">9</xref>] - [<xref ref-type="bibr" rid="scirp.88699-ref14">14</xref>] , anomalous ligaments [<xref ref-type="bibr" rid="scirp.88699-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref15">15</xref>] or conditions affecting other extraocular muscles [<xref ref-type="bibr" rid="scirp.88699-ref13">13</xref>] . It has even been suggested that BS could be included in the denominated Congenital Cranial Denervation Diseases [<xref ref-type="bibr" rid="scirp.88699-ref16">16</xref>] , which would help to explain the high frequency of iatrogenic BS after surgical correction of the cranial nerve IV paralysis [<xref ref-type="bibr" rid="scirp.88699-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref17">17</xref>] . However, a definitive etiological diagnosis is not possible without magnetic resonance imaging or exploratory surgery, so the disease is classified as idiopathic in most cases. Traumatic, inflammatory [<xref ref-type="bibr" rid="scirp.88699-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref20">20</xref>] or tumoral [<xref ref-type="bibr" rid="scirp.88699-ref21">21</xref>] entities should be considered and excluded.</p><p>No consensus has been reached regarding the best surgical treatment, but surgical intervention of the SO is the current mainstay. Tenotomies and tenectomies are popular because of their simplicity, but are less predictable and have a higher incidence of consecutive SO paresis than lengthening techniques [<xref ref-type="bibr" rid="scirp.88699-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref22">22</xref>] . The purpose of the latter techniques is to lengthen the tendon without causing consecutive paresis and, ideally, to do so in a reversible way.</p><p>One popular lengthening technique is SO weakening with a bridge suture technique, between 3 and 8 mm. It is an effective and safe procedure but may be associated with local fibrosis, causing late undercorrections [<xref ref-type="bibr" rid="scirp.88699-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref24">24</xref>] .</p><p>An alternative to this technique is the use of a silicone band, that can be more stable but is also associated with complications, including consecutive paralysis, adhesion of the band to the adjacent tissues and spontaneous implant extrusion [<xref ref-type="bibr" rid="scirp.88699-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref27">27</xref>] .</p><p>Surgical correction is usually not necessary, as spontaneous improvement is described in 6% to 90% of cases, depending on the studies [<xref ref-type="bibr" rid="scirp.88699-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref30">30</xref>] . Therefore, a conservative approach is usually recommended [<xref ref-type="bibr" rid="scirp.88699-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref32">32</xref>] .</p><p>In this study, we analyze the cases of Brown’s Syndrome of our department and report their clinical progression and outcome.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>The cases diagnosed as Brown’s Syndrome in the Strabismus Department of Instituto de Oftalmologia Dr. Gama Pinto between 1983 and 2014 were retrospectively reviewed. The study was conducted in accordance with the tenets of the Declaration of Helsinki and approved by the Ethics Commission for Healthcare of Instituto de Oftalmologia Dr. Gama Pinto. Informed consent was obtained from all participants or their parents.</p><p>Data was collected, namely epidemiology, diagnosis and follow-up dates, extraocular motility, ocular deviations, anomalous head position, visual acuity, refraction, and treatment.</p><p>The deviations were measured using the prismatic Cover Test.</p><p>Visual acuity was evaluated with Snellen optotypes scale, Snellen EE scale or Sheridan test, according to age and cooperation of the patient [<xref ref-type="bibr" rid="scirp.88699-ref33">33</xref>] .</p><p>Brown’s Syndrome was diagnosed when an incomitant strabismus affecting elevation in adduction was present.</p><p>Surgical plans were made at the discretion of the surgeon. All surgeries were performed by the same surgeon over this 31 years period.</p></sec><sec id="s3"><title>3. Results</title><p>We reviewed 39 cases of BS. Every case was included in the study, considering that complete data was present in at least 4 moments: at diagnosis, pre-operatively, post-operatively and final observation. However, when analyzing the natural history, cases with a follow-up inferior to 1 year were excluded.</p><p>Six of the cases were iatrogenic, consecutive to SO tuck surgery in the context of congenital IV cranial nerve paralysis. In the remaining 33 cases, no defined etiology and no systemic causes or hereditary patterns were found.</p><p>Because of the inherent differences between iatrogenic and idiopathic cases, they will be described separately. Population characteristics may be found in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Some cases of idiopathic BS presented with ocular deviation in primary position, as shown in <xref ref-type="table" rid="table2">Table 2</xref>. Compensatory head position was present in 15 cases, including 4 cases with tilted head to the affected side, 3 with chin elevation, 1 with a head turn to the opposite side and 7 with a combination of the aforementioned positions.</p><p>All 8 cases diagnosed with amblyopia had horizontal deviations in the primary position, anisometropia or nystagmus, in addition to BS. Treatment with optical correction and occlusion was prescribed, resulting in complete recovery in 7 cases.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Population demographic and clinical data according to etiology</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Characteristic</th><th align="center" valign="middle"  colspan="4"  >Idiopathic group</th><th align="center" valign="middle"  colspan="4"  >Iatrogenic group</th></tr></thead><tr><td align="center" valign="middle" >OD</td><td align="center" valign="middle"  colspan="2"  >OS</td><td align="center" valign="middle" >OU</td><td align="center" valign="middle" >OD</td><td align="center" valign="middle"  colspan="2"  >OS</td><td align="center" valign="middle" >OU</td></tr><tr><td align="center" valign="middle" >Laterality</td><td align="center" valign="middle" >17 (52%)</td><td align="center" valign="middle"  colspan="2"  >14 (42%)</td><td align="center" valign="middle" >2 (6%)</td><td align="center" valign="middle" >2 (33%)</td><td align="center" valign="middle"  colspan="2"  >3 (50%)</td><td align="center" valign="middle" >1 (17%)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >Male</td><td align="center" valign="middle"  colspan="2"  >Female</td><td align="center" valign="middle"  colspan="2"  >Male</td><td align="center" valign="middle"  colspan="2"  >Female</td></tr><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle"  colspan="2"  >13 (39%)</td><td align="center" valign="middle"  colspan="2"  >20 (61%)</td><td align="center" valign="middle"  colspan="2"  >4 (67%)</td><td align="center" valign="middle"  colspan="2"  >2 (33%)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >Mean &#177; SD</td><td align="center" valign="middle"  colspan="2"  >[Min - Max]</td><td align="center" valign="middle"  colspan="2"  >Mean &#177; SD</td><td align="center" valign="middle"  colspan="2"  >[Min - Max]</td></tr><tr><td align="center" valign="middle" >AgeDiag</td><td align="center" valign="middle"  colspan="2"  >5.8 &#177; 8.6</td><td align="center" valign="middle"  colspan="2"  >[1 - 55]</td><td align="center" valign="middle"  colspan="2"  >6.5 &#177; 3.3</td><td align="center" valign="middle"  colspan="2"  >[4 - 13]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle"  colspan="2"  >Present</td><td align="center" valign="middle"  colspan="2"  >Absent</td><td align="center" valign="middle"  colspan="2"  >Present</td><td align="center" valign="middle"  colspan="2"  >Absent</td></tr><tr><td align="center" valign="middle" >AHP</td><td align="center" valign="middle"  colspan="2"  >15 (45.5%)</td><td align="center" valign="middle"  colspan="2"  >18 (54.5%)</td><td align="center" valign="middle"  colspan="2"  >0</td><td align="center" valign="middle"  colspan="2"  >6 (100%)</td></tr><tr><td align="center" valign="middle" >Amblyopia</td><td align="center" valign="middle"  colspan="2"  >8 (24%)</td><td align="center" valign="middle"  colspan="2"  >25 (76%)</td><td align="center" valign="middle"  colspan="2"  >0</td><td align="center" valign="middle"  colspan="2"  >6 (100%)</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>Age Diag―age at diagnosis; AHP―abnormal head position; OD―right eye; OS―left eye; OU―both eyes.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Ocular deviations in the idiopathic grou</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Deviation</th><th align="center" valign="middle" >Ortho</th><th align="center" valign="middle" >Ht &lt;10 D</th><th align="center" valign="middle" >Ht ≥10 D</th><th align="center" valign="middle" >ET &lt;10 D</th><th align="center" valign="middle" >ET 10 - 25 D</th><th align="center" valign="middle" >ET &gt;25 D</th><th align="center" valign="middle" >XT</th><th align="center" valign="middle" >Ht +ET</th><th align="center" valign="middle" >Ht +XT</th></tr></thead><tr><td align="center" valign="middle" >N= (%)</td><td align="center" valign="middle" >10 (30.3%)</td><td align="center" valign="middle" >5 (15.2%)</td><td align="center" valign="middle" >3 (9.1%)</td><td align="center" valign="middle" >1 (3%)</td><td align="center" valign="middle" >3 (9.1%)</td><td align="center" valign="middle" >1 (3%)</td><td align="center" valign="middle" >1 (3%)</td><td align="center" valign="middle" >4 (12.1%)</td><td align="center" valign="middle" >5 (15.2%)</td></tr></tbody></table></table-wrap><p>Ortho―orthotropia; Ht―hypotropia; ET―esotropia; XT―exotropia.</p><p>Three out of the 33 idiopathic cases abandoned follow-up within the period of 1 year, leaving a total of 30 cases that were followed for an average time of 6 years (1 - 16 years).</p><p>Surgical intervention was performed in 9 cases presenting with persistent hypotropia of at least 6D in the primary position. The age of intervention varied between 3 and 55 years, with a mean of 9 years and a median of 5 years.</p><p>The surgical goal was to correct the ocular deviation in the primary position and consequently to reduce or eliminate the associated torticollis.</p><p>Considering the idiopathic BS cases (cases 1 - 9 of <xref ref-type="table" rid="table3">Table 3</xref>), the surgery was successful in 7 cases. One case had complaints of diplopia several years later (case 4) and it was necessary to reoperate in 1 case, in order to perform a contralateral superior rectus weakening (case 6). Of the 2 unsuccessful cases: one was a late-onset BS with severe vertical diplopia that could not be corrected (case 9); and one was a child with a positive forced ductions test that was corrected right after the end of the surgery but that maintained the restriction of movements in the postoperative period (case 3).This patient is still under observation.</p><p>Twenty-one cases were kept under observation, with spontaneous improvement occurring in 13 (62%). This was shown by a progressive reduction of the restriction in supra-adduction and, in some cases, with near resolution of the limitation, especially during adolescence. Only 1 case showed a worsening of the condition, but without the development of amblyopia or abnormal head position, so surgical intervention was not performed. The remaining cases showed clinical stability. The characteristics of the idiopathic cases that showed improvement are compared in <xref ref-type="table" rid="table4">Table 4</xref>. Spontaneous improvement seems to be less likely in the presence of amblyopia. Although without statistical differences between the groups, horizontal deviations seem to be associated with a lower degree of spontaneous improvement.</p><p>Only 2 in 6 iatrogenic cases needed surgical correction, specifically, the reversion of the SO tuck that caused the condition. The surgery was successful in both cases (<xref ref-type="table" rid="table3">Table 3</xref>). The remaining 4 cases improved spontaneously, without the need for intervention.</p></sec><sec id="s4"><title>4. Discussion</title><p>We analyzed 39 cases of BS with different grades of severity and associated characteristics. We did not classify the cases as congenital or acquired due to difficulties in establishing the age of manifestation of the disease.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Surgeries performed and pre and post-op characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >N</th><th align="center" valign="middle"  colspan="4"  >Pre-op</th><th align="center" valign="middle"  rowspan="2"  >Surgery</th><th align="center" valign="middle"  colspan="4"  >Post-op</th></tr></thead><tr><td align="center" valign="middle" >VD</td><td align="center" valign="middle" >HD</td><td align="center" valign="middle" >AHP</td><td align="center" valign="middle" >Cl</td><td align="center" valign="middle" >VD</td><td align="center" valign="middle" >HD</td><td align="center" valign="middle" >AHP</td><td align="center" valign="middle" >Cl</td></tr><tr><td align="center" valign="middle" >1</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (8 mm)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >14 (XT)</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (7 mm)</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >4 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >30 (ET)</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (6 mm)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >4 (XT)</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (6 mm) + contralateral superior rectus recession</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >4 (XT)</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >5</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >8 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (6 mm) + contralateral superior rectus recession</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >4 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >6</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >16 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (4 mm) + ipsilateral superior rectus recession + contralateral inferior rectus recession</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >7</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO silicone band (8 mm) + contralateral superior rectus recession</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >8</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >25 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >Bilateral botulinum toxin in the medial rectus and subsequent bilateral medial rectus recession and posterior fixation suture + steroid injection in affected SO</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >9</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >8 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >SO bridge suture (8 mm) + ipsilateral lateral rectus recession + contralateral inferior oblique tenectomy + contralateral superior rectus recession</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >Tuck Reversion</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >11</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >6 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >Tuck Reversion + contralateral inferior oblique anteroposition to Fink’s point. Subsequently bilateral lateral rectus recession was performed.</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >10 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >12</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >16 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >Bilateral botulinum toxin in the medial rectus and subsequent medial rectus recession with posterior fixation suture</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >13</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >25 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >Bilateral botulinum toxin in the medial rectus</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >6 (ET)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >14</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >25 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >Bilateral lateral rectus recession</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >10 (XT)</td><td align="center" valign="middle" >A</td><td align="center" valign="middle" >1</td></tr></tbody></table></table-wrap><p>VD―vertical deviation in prism diopters; HD―horizontal deviation in prism diopters (XT―exotropia; ET―esotropia); AHP―abnormal head position (A―absent; P―present); Cl―classification of severity of BS (1 = mild, 2 = moderate, 3 = severe).</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Comparison of characteristics of idiopathic SB cases with and without spontaneous improvement</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >With spontaneous improvement</th><th align="center" valign="middle" >Without spontaneous improvement</th><th align="center" valign="middle" >p value</th></tr></thead><tr><td align="center" valign="middle" >Male/Female</td><td align="center" valign="middle" >7/6</td><td align="center" valign="middle" >2/6</td><td align="center" valign="middle" >0.195</td></tr><tr><td align="center" valign="middle" >OD/OS/OU</td><td align="center" valign="middle" >8/4/1</td><td align="center" valign="middle" >2/5/1</td><td align="center" valign="middle" >0.133</td></tr><tr><td align="center" valign="middle" >With/Without Amblyopia</td><td align="center" valign="middle" >1/12</td><td align="center" valign="middle" >5/3</td><td align="center" valign="middle" >0.014</td></tr><tr><td align="center" valign="middle" >AHP present/absent</td><td align="center" valign="middle" >5/7</td><td align="center" valign="middle" >3/5</td><td align="center" valign="middle" >0.596</td></tr><tr><td align="center" valign="middle" >Age Diag (years)</td><td align="center" valign="middle" >4.46 &#177; 2.18</td><td align="center" valign="middle" >4.38 &#177; 1.92</td><td align="center" valign="middle" >0.928</td></tr><tr><td align="center" valign="middle" >Vert Dev (D)</td><td align="center" valign="middle" >3.62 &#177; 6.24</td><td align="center" valign="middle" >2.29 &#177; 4.07</td><td align="center" valign="middle" >0.619</td></tr><tr><td align="center" valign="middle" >Esotropia (D)</td><td align="center" valign="middle" >1.08 &#177; 3.88</td><td align="center" valign="middle" >5.50 &#177; 10.41</td><td align="center" valign="middle" >0.281</td></tr><tr><td align="center" valign="middle" >Exotropia (D)</td><td align="center" valign="middle" >0.92 &#177; 3.33</td><td align="center" valign="middle" >3.75 &#177; 10.61</td><td align="center" valign="middle" >0.377</td></tr></tbody></table></table-wrap><p>Discrete variables are presented as the absolute number for each category and comparison is made with the chi-square test. Continuous variables are presented as mean &#177; standard deviation and comparison is made with the independent samples T test. Age Diag―age at diagnosis; AHP―abnormal head position; OD―right eye; OS―left eye; OU―both eyes.</p><p>We could not find the etiology of the disease, with the exception of the iatrogenic cases, so most cases were considered idiopathic.</p><p>Amblyopia was essentially associated with more amblyogenic pathologies (mostly esotropia or exotropia) and had a good therapeutic response.</p><p>Sixty-eight percent of the cases that were kept under observation showed spontaneous improvement, with the remaining maintaining stability. This is consistent with the data found in the literature [<xref ref-type="bibr" rid="scirp.88699-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref34">34</xref>] and strengthens the current recommendation of a conservative approach to these cases.</p><p>Despite the good prognosis, it is necessary to be alert to the presence of abnormal head position, which is probably underdiagnosed [<xref ref-type="bibr" rid="scirp.88699-ref35">35</xref>] , and had a significant prevalence in our population.</p><p>Regarding surgical treatments, the SO bridge suture was the most commonly used technique, because of the effectiveness and predictability described in the literature [<xref ref-type="bibr" rid="scirp.88699-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.88699-ref24">24</xref>] . The global surgical success was 78%, confirming the good results of this procedure. This technique was frequently combined with surgery in other muscles and, despite the complexity associated with this kind of procedure, the efficacy was good. Although surgery is not necessary in most cases, it should not be postponed when justified, as it allows for acceptable correction of primary position ocular alignment and the correction of abnormal head position, leading to improvements in quality of life.</p><p>Limitations of this study include its retrospective nature and varying times of follow-up that could interfere with the analysis. The surgical intervention was personalized to each patient, making it hard to compare techniques and to report global results.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, our experience seems to confirm that the spontaneous improvement of BS is common. This fact should be considered when evaluating BS. Furthermore, when surgery is required, planning may be complex, but the results are usually good.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>All authors declare that they have no conflict of interest.</p></sec><sec id="s7"><title>Ethical approval</title><p>All procedures performed were in accordance with the ethical standards of the institutional research committee and with the 1964 Declaration of Helsinki and its later amendments.</p></sec><sec id="s8"><title>Informed Consent</title><p>Informed consent was obtained from all individual participants included in the study.</p></sec><sec id="s9"><title>Cite this paper</title><p>Rodrigues, P.F., Seldon, R., Varandas, G. and Vieira, M.L. (2018) Natural History and Treatment of Brown’s Syndrome: Long-Term Experience. 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