| Literature DB >> 22786695 |
Yimin Zhu1, Ke Jin, Haibo Mei, Liping Li, Zheng Liu, Yongjia Yang, Jingsong Tang, Xielin He, Rui Zhao, Xinyu He.
Abstract
We report on a three-generation Chinese family presenting with a recognizable condition consisting of radio-ulnar synostosis, short stature, scoliosis, distinctive craniofacial features (thick vermilion to the lips, prominent eyes, and flat malar region), and a shortened and thickened femur neck. The inheritance of the trait was presumably autosomal dominant. The lack of microcephaly in the family suggested a variant of Giuffè-Tsukahara syndrome but could represent variabilityEntities:
Mesh:
Year: 2012 PMID: 22786695 DOI: 10.1002/ajmg.a.35478
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802