Isolated Ectopia Lentis in Suspect of Weill-Marchesani Syndrome (WMS)
نویسندگان
چکیده
Introduction: The prevalence of Weill-Marchesani syndrome (WMS) is estimated to be 1:100.000 proportion the population. Knowledge clinical and therapy WMS expected improve ability diagnose this disease. In case report, we will present a in tertiary hospital because our findings are rare essential concerning symptomatic treatment visual rehabilitation. Case Presentation: A 7-year-old child presented with blurred vision left eye. patient showed an abnormal facial appearance short stature brachydactyly on both hands. had history Intracapsular cataract extraction (ICCE) surgery right eye indication anterior lens subluxation. then suffered aphakic glaucoma after surgery. Anterior segment examination found lens, conjunctival sclerectasia, atrophic iris, mid-dilation pupil. iris From ocular disturbance, such as stature, was diagnosed suspected WMS. treated ICCE micropulse transscleral cyclophotocoagulation (MP-TSCPC) Conclusion: It make early diagnosis ectopia lentis patients it affect their vision.
منابع مشابه
[Weill-Marchesani syndrome].
Weill-Marchesani syndrome is a rare systemic connective tissue disease characterized by short stature, brachydactyly, ectopia lentis and spherophakia. This was first reported by Weill in 1932 and subsequently well characterized by Marchesani in 1939(1). Genetically this syndrome often shows autosomal recessive inheritance. Frequent consanguinity between parents support this model. There have be...
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The Weill-Marchesani syndrome is a rare systemic connective tissue disease characterised by small stature, brachydactyly, ectopia lentis, and spherophakia. Three siblings with typical manifestations of this syndrome were reported. The ophthalmological findings in all these cases were spherophakia, severe myopia, a shallow anterior chamber, and narrow angle glaucoma. Two cases underwent laser ir...
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eill-Marchesani syndrome (WMS) is a rare connective tissue disorder characterized by short stature, restricted movements of the fingers and brachydactyly. Most of these patients are referred to the ophthalmologist with features such as microspherophakia, lens dislocation, severe myopia, acute or chronic glaucoma, and cataract.1,2 Although either autosomal dominant or autosomal recessive inherit...
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ژورنال
عنوان ژورنال: Vision Science and Eye Health Journal
سال: 2022
ISSN: ['2809-218X']
DOI: https://doi.org/10.20473/vsehj.v2i1.2022.11-16