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伴有痴笑性癫痫、性早熟和多指畸形的下丘脑错构瘤。

Hypothalamic hamartoma with gelastic epilepsy, precocious puberty and polydactyly.

作者信息

Turanli G, Aynaci M, Yalnizoğlu D, Renda Y

机构信息

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.

出版信息

Turk J Pediatr. 1996 Oct-Dec;38(4):533-6.

PMID:8993186
Abstract

An entity including gelastic epilepsy, precocious puberty, polydactyly and a hypothalamic hamartoma type IIa is described in a 16-year-old female patient. Polydactyly was detected at birth, she developed precocious puberty at four years of age, and gelastic epilepsy was diagnosed at age seven. The precocious puberty was successfully treated medically and her treatment was discontinued at the age of 10 years, but the gelastic seizures were difficult to control. When the patient was 11 years old, MRI revealed a hypothalamic hamartoma. The combination of these four features is very rare in the literature.

摘要

一名16岁女性患者被描述为患有包括痴笑性癫痫、性早熟、多指畸形和IIa型下丘脑错构瘤的病症。患者出生时即被发现多指畸形,4岁时出现性早熟,7岁时被诊断为痴笑性癫痫。性早熟通过药物治疗成功治愈,10岁时停止治疗,但痴笑性癫痫难以控制。患者11岁时,磁共振成像(MRI)显示有下丘脑错构瘤。这四种特征的组合在文献中非常罕见。

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