胎儿苯妥英综合征：一例报告

Fetal hydantoin syndrome: a case report.

作者信息

Nanda A, Kaur S, Bhakoo O N, Kapoor M M, Kanwar A J

机构信息

Department of Dermatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Pediatr Dermatol. 1989 Jun;6(2):130-3. doi: 10.1111/j.1525-1470.1989.tb01011.x.

DOI:10.1111/j.1525-1470.1989.tb01011.x

PMID:2501774

Abstract

An infant with features of fetal hydantoin syndrome, born to an epileptic mother, was followed from birth to 20 months of age. Physical findings included gum hypertrophy, digitalization of the thumbs, hypoplasia of the distal phalanges and nails, epicanthal folds, pseudohypertelorism, epidermoid cyst, and geographic tongue. Available literature about the disorder is reviewed.

摘要

一名患有胎儿苯妥英综合征的婴儿，其母亲为癫痫患者，从出生起一直随访至20个月大。体格检查发现包括牙龈增生、拇指呈杵状、远端指骨和指甲发育不全、内眦赘皮、假性眼距过宽、表皮样囊肿和地图舌。本文对该疾病的现有文献进行了综述。