Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen.
Am J Med Genet
; 37(2): 272-6, 1990 Oct.
Article
em En
| MEDLINE
| ID: mdl-1978986
ABSTRACT
A mild autosomal dominant form of spondyloepiphyseal dysplasia (SED) is present in several generations of a South African family of English stock. This phenotype differs from that of any other previously described. Although type II collagen defects have been found in some families with SED congenita, the phenotype in our family showed discordant segregation with COL2A1 gene associated restriction fragment length polymorphisms (RFLPs), the markers for the structural locus of type II collagen. It is evident that the SED group of disorders is heterogeneous.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Osteocondrodisplasias
/
Colágeno
Limite:
Adolescent
/
Adult
/
Aged
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Idioma:
En
Revista:
Am J Med Genet
Ano de publicação:
1990
Tipo de documento:
Article