三名连续出生的兄弟姐妹患弗雷泽综合征。
Fraser syndrome in three consecutive siblings.
作者信息
Kalaniti Kaarthigeyan, Sandhya V
机构信息
Department of Pediatrics and Neonatal Medicine, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, India.
出版信息
Oman J Ophthalmol. 2011 May;4(2):87-9. doi: 10.4103/0974-620X.83661.
Abstract
Fraser syndrome (FS) is a rare disorder characterized by a combination of acrofacial and urogenital malformations with or without cryptophthalmos. We report a newborn and its two elder siblings who had multiple congenital anomalies and clinico-radiological features consistent with FS.
摘要
弗雷泽综合征（FS）是一种罕见的疾病，其特征为伴有或不伴有隐眼畸形的头面部和泌尿生殖系统畸形。我们报告了一名新生儿及其两名年长的兄弟姐妹，他们有多种先天性异常，临床和放射学特征与弗雷泽综合征相符。
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