Kallmann syndrome and hypogonadotropic hypogonadism do not exist as distinct conditions.
2.
The term congenital hypogonadotropic hypogonadism ( CHH ) is now often used.
3.
These characteristics are known as hypogonadotropic hypogonadism.
4.
Loss of DAX1 function leads to adrenal insufficiency and hypogonadotropic hypogonadism, which are the main characteristics of this disorder.
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Kallmann syndrome ( KS ) and other forms of hypogonadotropic hypogonadism ( HH ) are classed as pituitary or endocrine disorders.
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Other terms used include idiopathic / isolated hypogonadotropic hypogonadism ( IHH ), normosmic hypogonadotropic hypogonadism ( nHH ) or hypothalamic hypogonadism.
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Other terms used include idiopathic / isolated hypogonadotropic hypogonadism ( IHH ), normosmic hypogonadotropic hypogonadism ( nHH ) or hypothalamic hypogonadism.
8.
Individuals with Kallmann syndrome experience anosmia ( lack of smell ) and do not go through puberty ( hypothalamic hypogonadotropic hypogonadism ).
9.
This condition results from the enlarging tumor interfering with the normal function of gonadotropin pituitary cells resulting in secondary hypogonadotropic hypogonadism and infertility.
10.
Other genes are known to cause this condition, called idiopathic hypogonadotropic hypogonadism, and scientists do not think they have found all of its causes.
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