Concept information
Endocrine System Diseases
Gonadal Disorders
Disorders of Sex Development
46, XX Disorders of Sex Development
...
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
...
Male Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
...
Congenital Abnormalities
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
...
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
Gonadal Dysgenesis
Término preferido
Gonadal Dysgenesis, 46,XX
Notice: Undefined index: in /var/www/html/model/Concept.php on line 545
Tipo
-
mesh:Descriptor
Definición
- The 46,XX gonadal dysgenesis may be sporadic or familial. Familial XX gonadal dysgenesis is transmitted as an autosomal recessive trait and its locus was mapped to chromosome 2. Mutation in the gene for the FSH receptor (RECEPTORS, FSH) was detected. Sporadic XX gonadal dysgenesis is heterogeneous and has been associated with trisomy-13 and trisomy-18. These phenotypic females are characterized by a normal stature, sexual infantilism, bilateral streak gonads, amenorrhea, elevated plasma LUTEINIZING HORMONE and FSH concentration.
Concepto genérico
Etiquetas alternativas
- Gonadal Dysgenesis, 46, XX
- Gonadal Dysgenesis, XX Type
En otras lenguas
-
francés
-
Dysgénésie gonadique 46,XX
URI
http://data.loterre.fr/ark:/67375/JVR-DWR914QT-G
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}