| Literature DB >> 20503334 |
Bertrand Isidor1, Sabine Baron, Philippe Khau van Kien, Anne-Marie Bertrand, Albert David, Martine Le Merrer.
Abstract
This report describes two unrelated boys presenting with short stature, femoral metaphyseal abnormalities, platyspondyly, and retinitis pigmentosa. Patients share similar findings with cases described by Ehara et al. [Ehara et al. (1997); Eur J Pediatr 156:627-630] described as axial spondylometaphyseal dysplasia. The presence of consanguinity in one of our patients further supports an autosomal recessive mode of inheritance of what, we believe, constitutes a separate and distinct entity. (c) 2010 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 20503334 DOI: 10.1002/ajmg.a.33397
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802