伴有骶骨发育不全的克-费二氏综合征：一种额外的亚型，IV型。
Klippel-Feil anomaly with sacral agenesis: an additional subtype, type IV.
作者信息
Raas-Rothschild A, Goodman R M, Grunbaum M, Berger I, Mimouni M
机构信息
Department of Pediatrics B, Beilinson Medical Center, Tel Hashomer, Israel.
出版信息
J Craniofac Genet Dev Biol. 1988;8(4):297-301.
PMID:3065353
Abstract
This report describes a child with the Klippel-Feil anomaly and sacral agenesis. A review of the literature revealed that this association has been recorded on other occasions. We believe that this combination of findings is significant and thus propose to call this the Klippel-Feil anomaly type IV.
摘要
本报告描述了一名患有克-费二氏畸形和骶骨发育不全的儿童。文献回顾显示，这种关联在其他病例中也曾有记录。我们认为这一组合发现具有重要意义，因此提议将其称为克-费二氏畸形IV型。
Zotero 插件