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Kallmann Franz Josef, U.S. Medical geneticist and psychiatrist, 1897-1965.
See: Kallmann's syndrome.
(05 Mar 2000)
kallmann syndrome <syndrome> Congenital and familial disorder characterised by hypogonadotropic hypogonadism, eunuchoidal features, and anosmia or hyposmia. It is caused by a defect in the synthesis and/or release of lhrh (luteinizing hormone-releasing hormone; gonadorelin) from the hypothalamus as a result of faulty embryonic neuronal migration. The gene responsible for this is found in the region xp22.3 on the short arm of the x chromosome. There is a homolog on the y chromosome. The syndrome is more prevalent in males by a ratio of three to one.
(12 Dec 1998)
Kallmann's syndrome Failure of sexual development secondary to inadequate secretion of pituitary gonadotropins, associated with anosmia due to agenesis of the olfactory lobes of the brain; probably X-linked inheritance.
Synonym: Kallmann's syndrome.
(05 Mar 2000)
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