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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
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc1a/3160077/a27357d8e347/OJO-4-87-g001.jpg

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