Congenital GnRH deficiency Previous Next Congenital - TopicsExpress



          

Congenital GnRH deficiency Previous Next Congenital hypothalamic hypogonadism is usually only diagnosed in females when a delay in puberty is noted, as female infants are phenotypically normal. When associated with an absence of the sense of smell (anosmia) it is known as Kallman’s syndrome. It can be difficult to distinguish hypothalamic hypogonadism from delayed puberty; however, in the former, pubic hair is present as adrenarche occurs normally and children are usually of normal height for their age. Previous Next
Posted on: Fri, 04 Jul 2014 12:39:47 +0000

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