汉哈特综合征。
Hanhart syndrome.
作者信息
Dogan D G, Dogan M, Aslan M, Menekse E, Yakinci C
机构信息
Department of Pediatrics, Inönü University, Faculty of Medicine, Turgut Ozal Medical Center, Malatya, Turkey.
出版信息
Genet Couns. 2010;21(4):359-62.
PMID:21290964
Abstract
We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs.
摘要
我们报告了一名患有汉哈特综合征的男婴。它被归类于“口下颌肢体发育不全综合征”，这是一组罕见病症，涉及舌头、下颌骨和四肢的先天性畸形。
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