Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndrome.

IF 1.3 Q4 GENETICS & HEREDITY
Daiju Oba, Mariko Sagara, Sayuri Oda, Miyu Fukushima, Kenta Hasumi, Hirofumi Ohashi
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引用次数: 0

Abstract

Here we report an 18-year-old male patient with bilateral ectopia lentis and biallelic CPAMD8 variants (NM_015692.5:c.[2801delG];[4552C>T]; NP_056507.3:p.[(Gly934GlufsTer64)];[(Gln1518Ter)]). He exhibited previously unreported extraocular features, including a slender build, scoliosis, arachnodactyly and positive thumb sign and wrist sign, which is reminiscent of Marfan syndrome. These findings may suggest that CPAMD8-related disorder is a syndromic condition associated with extraocular systemic features similar to those seen in Marfan syndrome.

Abstract Image

与马凡氏综合征相关的异位晶状体患者的双等位基因camd8变异
在这里,我们报告了一位患有双侧异位晶状体和双等位基因CPAMD8变异的18岁男性患者(NM_015692.5:c.[2801delG];[4552C>T]; NP_056507.3:p.[(Gly934GlufsTer64)];[(Gln1518Ter)])。他表现出以前未报道的眼外特征,包括身材修长、脊柱侧凸、蛛网膜畸形、阳性拇指征和腕部征,这让人想起马凡综合征。这些发现可能表明,camd8相关疾病是一种与眼外系统特征相关的综合征,与马凡氏综合征相似。
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来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
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