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[伴有嗅觉缺失的家族性性腺功能减退:卡尔曼综合征]

[Familial hypogonadism with anosmia: Kallmann Syndrome].

作者信息

Brämswig J H, Schellong G, König A, Stubbe P

出版信息

Monatsschr Kinderheilkd. 1983 Apr;131(4):232-4.

PMID:6865980
Abstract

The familial occurrence of hypogonadism and anosmia (Kallmann-Syndrome) is reported in a 15 5/12 year old boy and his 20 7/12 year old sister, who in addition has a ventricular septal defect. To establish the diagnosis it is important to examine the patient with hypogonadism for anosmia since voluntary information is rarely obtained. Quite often there are additional, associated anomalies which have to be searched for carefully.

摘要

据报道,一名15又5/12岁的男孩及其20又7/12岁的姐姐患有性腺功能减退和嗅觉缺失(卡尔曼综合征),姐姐还伴有室间隔缺损。对于性腺功能减退患者,检查其是否存在嗅觉缺失对于确诊很重要,因为很少能获得患者主动提供的相关信息。通常还存在其他相关异常,必须仔细查找。

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