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 contributed equa...

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Autori principali:	Lin Z, Zhu M, Deng H
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Dove Medical Press 2021-04-01
Serie:	Risk Management and Healthcare Policy
Soggetti:	weill–marchesani syndrome microspherophakia ectopia lentis ltbp2 compound heterozygous secondary glaucoma
Accesso online:	https://www.dovepress.com/a-pedigree-report-of-a-rare-case-of-weillndashmarchesani-syndrome-with-peer-reviewed-fulltext-article-RMHP
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