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Am J Med Genet A ; 127A(3): 318-20, 2004 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-15150788

RESUMEN

Fibrochondrogenesis is one of the rare lethal osteochondrodysplasias, which show abnormal maturation, and disturbed growth of cartilage and bones. These disorders are a heterogenous group of genetic disorders with a total incidence of 1-3 in 10,000 births. Only 13 cases of fibrochondrogenesis have been published since Lazzaroni-Fossati et al. [1978] first described the disorder. We report on two sibs that occurred in a consanguineous couple and discuss the ultrasonographic, clinical, radiological, and pathological characteristics of this disorder. This occurrence confirms autosomal recessive inheritance of fibrochondrogenesis.


Asunto(s)
Osteocondrodisplasias/diagnóstico , Hermanos , Consanguinidad , Resultado Fatal , Humanos , Osteocondrodisplasias/diagnóstico por imagen , Osteocondrodisplasias/patología , Ultrasonografía
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