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Indian J Pediatr ; 2005 Apr; 72(4): 355-7
Artigo em Inglês | IMSEAR | ID: sea-82571

RESUMO

Fibrochondrogenesis is a rare lethal short-limb skeletal dysplasia. Till now only fifteen cases have been reported since Lazzaroni-Fossati first described it in 1978. Hence reported a case of fibrochondrogenesis in a child born to a consanguineously married couple with characteristic physical and radiological features and discuss the incidence, inheritance, ultrasonographic, clinical, radiological and pathological characteristics of this disorder.


Assuntos
Consanguinidade , Nanismo/diagnóstico , Genes Recessivos , Humanos , Recém-Nascido , Masculino , Osteocondrodisplasias/diagnóstico
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