| 영문 | hypogonadism | 한글 | 생식샘기능저하증 |
|---|---|---|---|
| 설명 | 정상적인 남성 및 여성이 되기 위해서는 시상하부에서 생식샘방출호르몬, 뇌하수체에서 황체호르몬과 난포자극호르몬, 고환에서는 오스털러움 난소에서는 에스트로겐과 포르게스테론이 분비되어야 한다. 생식샘기능저하증은 이러한 기전 중 일부가 결핍되어 성적으로 어린이의 상태를 벗어나지 못한 성적유치 내지 기능 저하된 경우를 말한다. |
||
| IHH | idiopathic hypogonadotropic hypogonadism; idiopathic hypothalamic hypogonadism; infectious human hep... |
|---|---|
| AHH | alpha-hydrazine analog of histidine; anosmia and hypogonadotropic hypogonadism [syndrome]; arylhydro... |
| HH | halothane hepatitis; hard-of-hearing; healthy hemophiliac; healthy human; hiatal hernia; holistic he... |
| HE | half-scan with extrapolation; hard exudate; hektoen enteric [agar]; hemagglutinating encephalomyelit... |
| FHH | Familial Hypocalciuric Hypercalcemia = Familial Benign Hypercalcemia |
| HH | Hypogonadotropic Hypogonadism |
|---|---|
| IHH | Isolated hypogonadotropic hypogonadism |
| HHG | Hypogonadotrophic hypogonadism |
| IHH | Idiopathic hypogonadotrophic hypogonadism |
| BFNC | Benign Familial Neonatal Convulsions |
| familial hypogonadotropic hypogonadism | A group of disorders characterised by failure of sexual development, owing to inadequate secretion of pituitary gonadotropins; perhaps X-linked or autosomal recessive inheritance. (05 Mar 2000) |
|---|
| hypogonadotropic hypogonadism | Defective gonadal development or function, or both, resulting from inadequate secretion of pituitary gonadotropins. Synonym: hypogonadotropic eunuchoidism, secondary hypogonadism. (05 Mar 2000) |
|---|---|
| hypogonadotropic | Indicating inadequate secretion of gonadotropins and its consequences. (05 Mar 2000) |
| hypogonadotropic eunuchoidism | Defective gonadal development or function, or both, resulting from inadequate secretion of pituitary gonadotropins. Synonym: hypogonadotropic eunuchoidism, secondary hypogonadism. (05 Mar 2000) |
| male hypogonadism | A state in which testes are present but fail to function normally; may be of gonadal or pituitary origin. Synonym: eunuchism, male hypogonadism. Hypergonadotropic eunuchoidism, eunuchoidism of gonadal origin, commonly accompanied by enhanced levels of pituitary gonadotropins in the blood and urine, as in Klinefelter's syndrome. (05 Mar 2000) |
| primary hypogonadism | Defective gonadal development or function, or both, due to abnormality or loss of the gonad itself. (05 Mar 2000) |
| secondary hypogonadism | Defective gonadal development or function, or both, resulting from inadequate secretion of pituitary gonadotropins. Synonym: hypogonadotropic eunuchoidism, secondary hypogonadism. (05 Mar 2000) |
| hypergonadotropic hypogonadism | Defective gonadal development or function of the gonads, resulting from elevated levels of gonadotropins. (05 Mar 2000) |
| hypogonadism | <endocrinology> A condition resulting from or characterised by abnormally decreased functional activity of the gonads, with retardation of growth and sexual development. (18 Nov 1997) |
| hypogonadism with anosmia | 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) |
| hypothalamic obesity with hypogonadism | A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms. Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism. Origin: L. Fr. G. Dys-, bad, + trophe, nourishment (05 Mar 2000) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| cancer, breast, familial | A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer. (12 Dec 1998) |
| paralysis, familial periodic | An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis). (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|