| Literature DB >> 2287543 |
R N Sener1, B S Sayli, U E Isikan, A R Ormeci, M Unsal, M Tigdemir.
Abstract
We present, a family manifesting a variation of the syndrome of ectrodactyly with tibial apasia. The principal case in the family showed the most severe bilateral skeletal malformations of this syndrome. The hand changes of this case (tetra-oligodactyly with missing 5th rays) and of a relative (oligodactyly with the last 3 rays being affected) reflected a variable manifestation of "ectrodactyly". Additionally, a review of the relevant literature is presented for further delineation of various aspects of this syndrome.Entities:
Mesh:
Year: 1990 PMID: 2287543 DOI: 10.1007/bf02010817
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449