| Literature DB >> 8011531 |
B Brichard1, C Vermylen, J M Scheiff, J L Michaux, J Ninane, G Cornu.
Abstract
This report describes the cases of two young female patients with congenital dyserythropoietic anaemia (CDA) type I who presented similar hand and foot skeletal abnormalities: lack of distal phalanges and nails, and syndactyly. Up to now, some morphological malformations have been described in association with CDA type I but there is no report of skeletal defects. These two cases are suggestive of a possible association between this hereditary anaemia and specific skeletal abnormalities of the distal extremities.Entities:
Mesh:
Year: 1994 PMID: 8011531 DOI: 10.1111/j.1365-2141.1994.tb03278.x
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998