4.0 Article

Cataract in You-Hoover-Fong syndrome: TELO2 deficiency

期刊

OPHTHALMIC GENETICS
卷 41, 期 6, 页码 656-658

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/13816810.2020.1821382

关键词

You-Hoover-Fong syndrome; TELO2; pediatric cataract; developmental delay; microcephaly

资金

  1. Instituto de Salud Carlos III: ISCIII [FIS P118/00111]
  2. FondoEuropeo de desarrollo regional (FEDER)

向作者/读者索取更多资源

Introduction Recently, You, Hoover-Fong, and colleagues described a disease caused by a deficiency of the telomere maintenance 2 gene (TELO2) function. The clinical spectrum includes early-onset global delay, dysmorphic facial features, auditory disorder, and reduced vision. Materials and methods We report two siblings, diagnosed with You-Hoover-Fong syndrome at the age of 28 and 14 months. Both were genetically studied to find the cause of their developmental delay and microcephaly. Results The identical compound heterozygous missense mutations in theTELO2gene were found in each. Ophthalmologically, both siblings were diagnosed with progressive congenital bilateral nuclear-lamellar cataracts. Conclusions We report nuclear-lamellar cataracts in two siblings diagnosed with You-Hoover-Fong syndrome.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据