Barr M, Heidelberger K P, Comstock C H
Department of Pediatrics, University of Michigan, Ann Arbor 48109, USA.
Am J Med Genet. 1995 Sep 25;58(4):348-52. doi: 10.1002/ajmg.1320580409.
We report on two sisters with an unusual form of craniosynostosis, protruding nasal spine, micrognathia, short limbs, lung hypoplasia, absent or hypoplastic gallbladder, short intestine with ileal distention, hypoplastic uterus, and intrauterine growth retardation. This combination of defects appears to be a newly recognized and probably autosomal recessive disorder.
我们报告了两姐妹患有一种不寻常形式的颅缝早闭、鼻棘突出、小颌畸形、四肢短小、肺发育不全、胆囊缺如或发育不全、小肠短小伴回肠扩张、子宫发育不全以及宫内生长迟缓。这种缺陷组合似乎是一种新发现的且可能为常染色体隐性遗传的疾病。