| Literature DB >> 846766 |
Abstract
A 6-year follow-up of a Greek girl with pycnodysostosis associated with heterozygous beta-thalassemia is reported. Active rickets in infancy was superimposed on pycnodysostosis. In the family the autosomal recessive disease, pycnodysostosis, appeared in two of three siblings in combination with the autosomal dominant disease, thalassemia minor.Entities:
Mesh:
Year: 1977 PMID: 846766 DOI: 10.1007/BF00973984
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449