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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
|
| pubmed:dateCreated |
1990-2-2
|
| pubmed:abstractText |
The rare syndrome of embryonic testicular regression or agonadism with XY karyotype is described in this paper in a sibship of 7 including 3 cases of regression at a earlier time (in three amenorrheic sisters and on case of tardive and incomplete regression in a brother with bilateral testicular hypotrophy. The antigen H-Y is present in the three sisters. The pathogenesis of this syndrome, compared with that of pure gonadal dysgenesis is discussed.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0001-4079
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
173
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
709-14; discussion 714-5
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:2598069-Adolescent,
pubmed-meshheading:2598069-Child,
pubmed-meshheading:2598069-Dermatoglyphics,
pubmed-meshheading:2598069-Female,
pubmed-meshheading:2598069-Gonadal Dysgenesis,
pubmed-meshheading:2598069-Gonadal Dysgenesis, 46,XY,
pubmed-meshheading:2598069-Humans,
pubmed-meshheading:2598069-Karyotyping,
pubmed-meshheading:2598069-Lebanon
|
| pubmed:year |
1989
|
| pubmed:articleTitle |
[Familial testicular regression syndrome].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|