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利用患病同胞的一致性率对比默-兰格综合征进行进一步描述。

Further delineation of the Beemer-Langer syndrome using concordance rates in affected sibs.

作者信息

Lurie I W

机构信息

Department of Pediatrics, University of Maryland at Baltimore, School of Medicine.

出版信息

Am J Med Genet. 1994 May 1;50(4):313-7. doi: 10.1002/ajmg.1320500403.

Abstract

Six familial cases of the Beemer-Langer syndrome (BLS) were analyzed to further elucidate the spectrum and frequency of anomalies observed in this disorder. Preaxial polydactyly was found in 3/6 affected sibs, and, therefore, its frequency previously may have been underestimated. Some patients, described as infants affected with the Majewski syndrome (MS) or "atypical" short rib-polydactyly conditions, may indeed have BLS. A high frequency of brain defects (16/26) and cleft tongue, oral frenula, and/or natal teeth (13/29) widens the list of typical findings in this syndrome. The specific type of tibial defect seems to be the most important discrimination of the MS and the BLS.

摘要

对六例比默 - 兰格综合征(BLS)的家族病例进行了分析,以进一步阐明该疾病中观察到的异常范围和频率。在6名受影响的同胞中有3名发现了轴前多指畸形,因此其频率此前可能被低估了。一些被描述为患有马耶夫斯基综合征(MS)或“非典型”短肋多指畸形的婴儿患者,实际上可能患有BLS。脑缺陷(26例中有16例)以及舌裂、口腔系带和/或 natal 牙(29例中有13例)的高发生率扩大了该综合征典型表现的范围。胫骨缺陷的具体类型似乎是区分MS和BLS的最重要因素。

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