Document Detail

A new case of fibrochondrogenesis from Spain.
MedLine Citation:
PMID:  8733059     Owner:  NLM     Status:  MEDLINE    
A rare, neonatally lethal chondrodysplasia with histological characteristics was first described in 1978 and the authors named the condition fibrochondrogenesis. Here we report the eighth published case of fibrochondrogenesis. This was identified in a population of 1,158,067 consecutive livebirths, so we can assume that this figure should be the minimal prevalence for livebirths.
M L Martínez-Frías; A García; J Cuevas; J I Rodríguez; M Urioste
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of medical genetics     Volume:  33     ISSN:  0022-2593     ISO Abbreviation:  J. Med. Genet.     Publication Date:  1996 May 
Date Detail:
Created Date:  1996-10-10     Completed Date:  1996-10-10     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  2985087R     Medline TA:  J Med Genet     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  429-31     Citation Subset:  IM    
ECEMC, Facultad de Medicina, Universidad Complutens, Madrid, Spain.
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MeSH Terms
Abnormalities, Multiple* / pathology
Cervical Vertebrae / abnormalities,  radiography
Fatal Outcome
Infant, Newborn
Osteochondrodysplasias* / pathology,  radiography
Skull / abnormalities,  radiography

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