| Literature DB >> 8832138 |
D Concolino1, D Sperlì, R Cinti, P Strisciuglio, G Andria.
Abstract
Roberts syndrome is a rare autosomal recessive condition characterized by growth retardation, cranio-facial abnormalities and symmetrical limb reduction of variable severity. Most patients with Roberts syndrome show a typical cytogenetic finding known as "Roberts syndrome effect". We describe a 4-month-old patient with a mild form of this syndrome, who presented with an asymmetrical reduction of the right upper limb.Entities:
Mesh:
Year: 1996 PMID: 8832138 DOI: 10.1111/j.1399-0004.1996.tb03787.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438