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II型耳-腭-指综合征

Oto-palato-digital syndrome type II.

作者信息

Stoll C, Alembik Y

机构信息

Institut de puériculture, Centre hospitalier et Universitaire, Strasbourg, France.

出版信息

Genet Couns. 1994;5(1):61-6.

PMID:8031537
Abstract

We report a patient with a sporadic case of oto-palato-digital (OPD) syndrome type II. Parents and five previous sibs are normal. At 26 years of age the patient had conductive hearing impairment, cleft palate, a prominent forehead, a flat facies, and a broad nasal base resulting in the characteristic "pugilistic" appearance. Extension and supination were limited at the elbows; thumbs and halluces were broad. Many radiological abnormalities were noted: malformations of the cervical spine, pelvic abnormalities, bilateral coxa valga, genu valgum, small fibulae, pes equino varus, and 15 carpal bones. IQ improved dramatically from 65 to 95.

摘要

我们报告了一例散发的II型耳-腭-指(OPD)综合征患者。其父母及五个同胞均正常。该患者26岁时出现传导性听力障碍、腭裂、前额突出、面部扁平以及鼻基底宽阔,从而导致典型的“拳击手”面容。肘部伸展和旋后受限;拇指和拇趾宽阔。发现了许多放射学异常:颈椎畸形、骨盆异常、双侧髋外翻、膝外翻、腓骨短小、马蹄内翻足以及15块腕骨。智商从65显著提高到95。

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