无颌畸形、全前脑畸形与脏器反位：第三例报告
Agnathia, holoprosencephaly, and situs inversus: a third report.
作者信息
Meinecke P, Padberg B, Laas R
机构信息
Abteilung Medizinische Genetik, Altonaer Kinderkrankenhaus, Universität Hamburg, Federal Republic of Germany.
出版信息
Am J Med Genet. 1990 Oct;37(2):286-7. doi: 10.1002/ajmg.1320370226.
PMID:2248299
Abstract
We report on a male infant with cyclopia, agnathia, and situs inversus. In addition, anal atresia and horseshoe-kidneys were present. To our knowledge, this is the third published case of the "agnathia-holoprosencephaly-further midline defects association."
摘要
我们报告了一名患有独眼畸形、无下颌畸形和内脏反位的男婴。此外，还存在肛门闭锁和马蹄肾。据我们所知，这是第三例已发表的“无下颌畸形-前脑无裂畸形-其他中线缺陷关联症”病例。
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