A Pedigree Report of a Rare Case of Weill–Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations

A Pedigree Report of a Rare Case of Weill–Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations

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 Republic of China*These authors contribu...

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Bibliographic Details
Main Authors: Lin Z, Zhu M, Deng H
Format: Article
Language:English
Published: Dove Medical Press 2021-04-01
Series:Risk Management and Healthcare Policy
Subjects:
weill–marchesani syndrome
microspherophakia
ectopia lentis
ltbp2
compound heterozygous
secondary glaucoma
Online Access:https://www.dovepress.com/a-pedigree-report-of-a-rare-case-of-weillndashmarchesani-syndrome-with-peer-reviewed-fulltext-article-RMHP

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https://www.dovepress.com/a-pedigree-report-of-a-rare-case-of-weillndashmarchesani-syndrome-with-peer-reviewed-fulltext-article-RMHP

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