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弗雷泽综合征的家族内变异性。

Intrafamilial variability in Fraser syndrome.

作者信息

Prasun Pankaj, Pradhan Mandakini, Goel Himanshu

机构信息

Sanjay Gandhi Postgraduate Institute of Medical Sciences, Medical Genetics, India.

出版信息

Prenat Diagn. 2007 Aug;27(8):778-82. doi: 10.1002/pd.1774.

Abstract

Fraser syndrome (OMIM 219000) is a rare, autosomal recessive disorder characterized by cryptophthalmos, cutanaeous syndactyly, malformations of the larynx and genitourinary tract, craniofacial dysmorphism, orofacial clefting, mental retardation and musculoskeletal anomalies. There is marked interfamilial clinical heterogeneity. However, there is strong phenotypic similarity and concordance of the degree of severity of the disease within a family. We report a family with two cases of Fraser syndrome with marked clinical heterogeneity. One case had lethal phenotype with bilateral renal agenesis, while the other had mild phenotype with normal kidneys. It has not been reported before and highlights the importance of careful screening of pregnancies in families with Fraser syndrome.

摘要

弗雷泽综合征(OMIM 219000)是一种罕见的常染色体隐性疾病,其特征为隐眼畸形、皮肤并指(趾)畸形、喉和泌尿生殖道畸形、颅面畸形、口面裂、智力障碍及肌肉骨骼异常。家族间存在显著的临床异质性。然而,同一家庭内疾病的严重程度在表型上有很强的相似性和一致性。我们报告了一个有两例弗雷泽综合征的家庭,两例临床异质性显著。一例具有致死性表型,伴有双侧肾缺如,而另一例表型较轻,肾脏正常。此前未见报道,这凸显了对弗雷泽综合征家族妊娠进行仔细筛查的重要性。

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