Bartsocas-Papas Syndrome: Case Report

Author:

Nikhat Fareeda,Fernandes Shalini Dolly,Mashharawi Nabilah,Bahutair ShadhaORCID

Abstract

Bartsocas-Papas syndrome (BPS) is a rare form of autosomal recessive disease, which is often severe and most of the time lethal. Only a few cases have been reported in the literature, so far mainly from the Mediterranean ancestry. We are describing here a case of severe form of BPS, which we encountered in our hospital in Dubai, UAE, which was diagnosed by antenatal scan; the baby had typical features of BPS and died immediately within few hours of life. Parents were first-degree consanguineous couples, and there was a family history of this disorder.

Publisher

S. Karger AG

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Congenital ankyloblepharon in a newborn with an IRF6 mutation;Journal of American Association for Pediatric Ophthalmology and Strabismus;2023-02

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