无甲畸形合并缺指（趾）畸形综合征：1例报告
Anonychia associated with ectrodactyly syndrome: a case report.
作者信息
Patiroğlu T, Hasanoğlu E
出版信息
Turk J Pediatr. 1989 Jul-Sep;31(3):249-52.
PMID:2485992
Abstract
Anonychia with ectrodactyly is a rare inherited autosomal dominant syndrome. A case of a two-month-old female infant presenting with anonychia in association with ectrodactyly and microcephaly is presented.
摘要
无甲并指缺如综合征是一种罕见的常染色体显性遗传综合征。本文报告一例两个月大的女婴，表现为无甲并伴有指缺如和小头畸形。
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