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Fibrochondrogenesis.
Indian J Pediatr ; 2005 Apr; 72(4): 355-7
Article in English | IMSEAR | ID: sea-82571
ABSTRACT
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.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Osteochondrodysplasias / Humans / Male / Infant, Newborn / Consanguinity / Dwarfism / Genes, Recessive Language: English Journal: Indian J Pediatr Year: 2005 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Osteochondrodysplasias / Humans / Male / Infant, Newborn / Consanguinity / Dwarfism / Genes, Recessive Language: English Journal: Indian J Pediatr Year: 2005 Type: Article