Literature DB >> 10213049

Acrodysplasia, severe ossification abnormalities with short stature, and fibular hypoplasia.

A Castriota-Scanderbeg1, L Zelante, S Masala, P Gasparini, R S Lachman.   

Abstract

We present a girl with short stature, growth hormone neurosecretory dysfunction, severe hypoplastic/aplastic changes of the bones of the hands and feet with dysharmonic ossification, severely delayed bone age, microcrania, and fibular hypoplasia. Parental consanguinity suggests autosomal recessive inheritance. An additional three cases [Eiken et al., 1984: Eur J Pediatr 141: 231-235] sharing some of the radiographic manifestations of this patient have been reported. However, distinctive findings in the present case seem to outline a separate entity.

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Year:  1999        PMID: 10213049     DOI: 10.1002/(sici)1096-8628(19990507)84:1<68::aid-ajmg13>3.0.co;2-j

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Angel-shaped phalanges in brachydactyly C: a case report, and speculation on pathogenesis.

Authors:  Alessandro Castriota-Scanderbeg; Francesco Giuseppe Garaci; Giampiero Beluffi
Journal:  Pediatr Radiol       Date:  2004-11-23
  1 in total

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