Results 1 to 10 of about 6,475 (185)
Marfan syndrome associated to pectus carinatum: a case report from cartagena de indias. Colombia
Revista Ciencias Biomédicas, 2011 Marfan syndrome (MFS) is the most common connective tissue inherited disorder,transmitted as an autosomic dominant character. Mutation is located in FBN1 allele,that encodes to Fibrilin-1.
Malambo-García Dacia I +4 more
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Bilateral simple ectopia lentis
Indian Journal of Ophthalmology. Case Reports, 2023 Shagun Korla, Ravinder K Gupta
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Risk Management and Healthcare Policy, 2021 ZhiHong Lin,* MinJuan Zhu,* HongWei Deng Department of Strabismus & Pediatric Ophthalmology, Shenzhen Eye Hospital Affiliated to Jinan University, The School of Optometry of Shenzhen University, Shenzhen, 518000, Guangdong Province, People’s ...
Lin Z, Zhu M, Deng H
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A Weill–Marchesani Case Trilogy: Ocular and Systemic Features
TNOA Journal of Ophthalmic Science and ResearchWeill-Marchesani syndrome is a rare genetic condition. It occurs in one in 100,000 of the population. Presently, there is no universally accepted treatment modality. Removal of the microspherophakic lens is recommended to control intraocular pressure and
Sujit Das
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Ectopia lentis differential diagnosis
The Pan-American Journal of Ophthalmology, 2020 Jamir Pitton Rissardo +1 more
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Ectopia lentis in marfan syndrome
TNOA Journal of Ophthalmic Science and Research, 2021 Vijayalakshmi A Senthilkumar, P Vineela
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Symmetrical Nasal Ectopia Lentis
Asia-Pacific Journal of Ophthalmology, 2022 Xiaogang, Wang, Timothy P H, Lin
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