Isolated FSH deficiency (Q97196): Difference between revisions
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Transtorno raro de comprometimento da síntese/secreção do hormônio folículo-estimulante (FSH) pela glândula pituitária, manifestando-se com hipogonadismo hipogonadotrófico, usualmente causado por uma mutação no gene da subunidade beta do FSH. | |||
| description / en | description / en | ||
A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene. | |||
Revision as of 13:14, 16 August 2026
A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1431378723 |
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| English | Isolated FSH deficiency |
A rare disorder of impaired synthesis/secretion of follicle-stimulating hormone (FSH) in the pituitary gland, manifesting in hypogonadotropic hypogonadism, usually caused by a mutation of FSH beta subunit gene. |
