Literature DB >> 8011531

Two cases of congenital dyserythropoietic anaemia type I associated with unusual skeletal abnormalities of the limbs.

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.

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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


  2 in total

1.  Acral dysostosis dyserythropoiesis syndrome.

Authors:  M Le Merrer; R Girot; P Parent; V Cormier-Daire; P Maroteaux
Journal:  Eur J Pediatr       Date:  1995-05       Impact factor: 3.183

Review 2.  The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I.

Authors:  Noémi B A Roy; Christian Babbs
Journal:  Br J Haematol       Date:  2019-03-05       Impact factor: 6.998

  2 in total

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