比默-兰格型短肋多指综合征：两例报告。

Beemer-Langer type short rib-polydactyly syndrome: report of two cases.

作者信息

Tsai F J, Tsai C H, Wang T R

机构信息

Department of Pediatrics, China Medical College Hospital, Taichung, Taiwan, R.O.C.

出版信息

Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1994 Jul-Aug;35(4):331-4.

PMID:8085456

Abstract

Two sibs who died shortly after birth had multiple congenital anomalies that included hydrops, narrow thorax, short limbs, and absence of polydactyly; therefore short rib (polydactyly) syndrome Beemer-Langer type was suggested. We report these cases and discuss the differentiation with Majewski type.

摘要

两名出生后不久死亡的同胞兄弟姐妹患有多种先天性异常，包括水肿、胸廓狭窄、四肢短小和无多指畸形；因此，提示为短肋（多指）综合征Beemer-Langer型。我们报告这些病例并讨论与Majewski型的鉴别。