Holoprosencephaly, ventricular septal defect, and postaxial polydactyly in a human embryo.
作者信息
Shiota K, Tanimura T
出版信息
J Med Genet. 1988 Jul;25(7):502-3. doi: 10.1136/jmg.25.7.502.
Abstract
摘要
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Holoprosencephaly, ventricular septal defect, and postaxial polydactyly in a human embryo.一名人类胚胎中的前脑无裂畸形、室间隔缺损和轴后多指畸形。
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Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly.孕早期对一例患有胎儿前脑无裂畸形、鼻发育不全和轴后多指畸形的妊娠进行13三体阳性无创产前检测。
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Hypopituitarism in association with postaxial polydactyly.垂体功能减退合并轴后多指畸形。
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Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome.前脑无裂畸形和多指畸形：水脑致死综合征的一种可能表现。
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Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.前脑无裂畸形-多指（“假三体性13”）综合征：一种具有水脑致死综合征和史密斯-勒米-奥皮茨综合征特征的综合征。一项多中心合作研究。
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本文引用的文献
1
Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.不明综合征：全前脑畸形、先天性心脏缺陷和多指畸形。
J Med Genet. 1987 Nov;24(11):714-5. doi: 10.1136/jmg.24.11.714.
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