| KAL | Kallmann [syndrome] |
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| KS | Kallmann syndrome; Kaposi sarcoma; Kartagener syndrome; Kawasaki syndrome; keratan sulfate; ketoster... |
| Kallmann | Franz Josef, U.S. Medical geneticist and psychiatrist, 1897-1965. See: Kallmann's syndrome. (05 Mar 2000) |
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| 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) |
Synonyms : Kallmann Syndrome 1, Kallmann Syndrome 2, Kallmann's Syndrome, Syndrome, Kallmann, Syndrome, Kallmann's
| Kallmann's syndrome |
Congenital absence of gonadotropin releasing hormone in the hypothalamus (causing, in women, primary amenorrhea and anovulation and, in men, failure of puberty) in combination with a congenitally absent sense of smell.
출처: www.jansen.com.au/Dictionary_JL.html
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| Kallmann s. |
a type of hypogonadotropic hypogonadism caused by failure of fetal gonadotropin-releasing hormone neurons to migrate to the thalamus, usually associated with anosmia or hyposmia. It is usually passed by autosomal recessive inheritance, and some cases are x-linked.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Kallmann syndrome |
see under syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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