| 영문 | adrenal gland | 한글 | 부신 |
|---|---|---|---|
| 설명 | 콩팥위에 존재하는 피라밋모양의 구조물. 겉질과 속질로 되어 있으며 호르몬의 분비가 주역할이다.  |
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| 영문 | hypoplasia | 한글 | 형성저하증 |
|---|---|---|---|
| 설명 | 장기의 불완전한 발달 때문에 성인의 크기에 도달하지 못한 상태. 그 중증도는 무형성보다 가볍다. 개체의 발달과정에서 어떤 원인에 의해 장기조직의 형성이 불완전하게 되는 것을 말한다. 기관 원기는 존재하지만 발육이 불완전하게 끝난 상태이다. 대다수의 경우 원인은 불확실하지만, 원인으로서 생각되는 것으로는 유전, 감염, 영양장애, 내분비장애, 외상, 방사선 등을 들 수 있다. 장기조직이 정상적으로 형성된 뒤 그 체적이 감소해 가는 위축과는 구별된다. |
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| 영문 | adrenal medulla | 한글 | 부신속질 |
|---|---|---|---|
| 설명 | 부신의 안쪽에 있는 부분으로 부교감신경의 지배를 받아서 카테콜라민(catecholamine)을 분비한다. |
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| 영문 | thymus(gland) | 한글 | 가슴샘 |
|---|---|---|---|
| 설명 | 가슴의 앞 위쪽에 위치한 림프성 장기로서, 사춘기에 최고의 무게에 달했다가 이후에 퇴축한다. 이것은 세포매개 면역(cell-mediated immunity: 주로 T-림프구에 의해 일어나며, 자기와 다른 세포에 대한 인식과 이식거부반응에 관여함)기능의 발달과 성숙에 필요한 장기이며, 회백적색으로 보통 정중면에서 결합조직에 의해 결합된 두 개의 엽으로 되어 있다. 가슴샘은 상피세포, 림프구, 가슴샘세포로 구성되어 있으며 전구세포가 가슴샘에 이행하여 림프구로 분화되고, 그 대부분은 파괴되나 나머지는 T림프구를 형성한다. 가슴샘은 또한 호르몬 유사물질인 thymine, thymopoietin, thymosin 등을 분비한다. |
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| 영문 | thyroid gland | 한글 | 갑상샘 |
|---|---|---|---|
| 설명 | 사람의 몸에서 가장 큰 내분비샘으로 목의 앞쪽, 아래쪽에 위치하고 있으며 2엽으로 구성되어 있다. 각 엽은 기관의 양쪽에 있으며 좁은 잘룩에 의해 앞에서 연결되어 있다. 갑상샘호르몬인 티록신(thyroxine)을 분비하고 저장하며, 필요에 따라 방출한다. 또한 갑상샘은 티로칼시토닌(thyrocalcitonin)도 분비한다. 병적인 상태에서 크기가 대개 증가하고, 일부에서는 도리어 위축되며, 통증을 나타내기도 한다. |
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| TOF | 1) Tetralogy Of Fallot ? CIx of Corrective Op ... |
|---|---|
| PAGOD | pulmonary hypoplasia-hypoplasia of pulmonary artery-agonadism-omphalocele/diaphragmatic defect-dextr... |
| AH | abdominal hysterectomy; absorptive hypercalciuria; accidental hypothermia; acetohexamide; acid hydro... |
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| AHC | Adrenal hypoplasia congenita |
|---|---|
| CHH | Cartilage hair hypoplasia |
| FDH | Focal Dermal Hypoplasia |
| PH | Pulmonary hypoplasia |
| AA | Adrenal androgen |
| adrenal gland | <anatomy, endocrinology> This gland is found above each kidney and it made up of an outer wall (cortex) that secretes important steroid hormones and an inner portion (medulla) that produces adrenaline (adrenaline) and noradrenaline (noradrenaline). The hormones help control heart rate, blood pressure, the way the body uses food, and other vital functions. (25 Jun 1999) |
|---|---|
| adrenal gland hypofunction | Adrenocortical hypofunction includes all conditions in which adrenal steroid hormone secretion falls below the requirements of the body. Adrenal insufficiency may be divided into two general categories: (1) those associated with primary inability of the adrenal to elaborate sufficient quantities of hormone and (2) those associated with a secondary failure due to a primary failure in the elaboration of adrenocorticotropin. (12 Dec 1998) |
| adrenal gland insufficiency | <endocrinology> A condition that results from the inadequate production of adrenal hormones (see Addison's disease). (27 Sep 1997) |
| adrenal gland tumour | <oncology> A benign tumour or adenoma, that usually results in the excess production of adrenal gland hormones. (27 Sep 1997) |
| medulla of adrenal gland | It is composed principally of anastomosing cords of cells in the core of the gland; the cells display a chromaffin reaction because of the presence of epinephrine and norepinephrine in their granules. Synonym: medulla glandulae suprarenalis, medulla of adrenal gland. (05 Mar 2000) |
| parathyroids, hypoplasia of the thymusand | Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands which control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the heart involving the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome. (12 Dec 1998) |
| cartilage-hair hypoplasia | An autosomal recessive form of dwarfism characterised by shortness of the extremities without skull defects, and with sparse, brittle hair of light colour. There is a peculiar, not adequately explained severity in the clinical course of varicella and herpes in such patients. (05 Mar 2000) |
| renal hypoplasia | An abnormally small kidney that is morphologically normal but has either a reduced number of nephrons or smaller nephrons. (05 Mar 2000) |
| right ventricular hypoplasia | A congenital or acquired condition in which there is thinning of the right ventricular myocardium. Synonym: right ventricular hypoplasia. (05 Mar 2000) |
| hypoplasia | <embryology> The incomplete development or underdevelopment of an organ or tissue. Origin: Gr. Plasis = formation (18 Nov 1997) |
| hypoplasia of right ventricle | Failure of development of the right ventricle resulting in its having little muscle and much connective tissue instead of the reverse. (05 Mar 2000) |
| hypoplasia of the thymus and parathyroids | Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands needed to control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome (since the faulty structures in dgs are embryologically derived from the third and fourth pharyngeal pouches). (12 Dec 1998) |
| dental enamel hypoplasia | <dentistry> A form of amelogenesis imperfecta characterised by incomplete formation of the dental enamel and transmitted as an x-linked or autosomal dominant trait. It is also associated with vitamin a, c, or d deficiency, infectious disease, prematurity, birth injury, rh incompatibility, trauma, or local infection. Small grooves, pits, and fissures are seen in mild cases, deep horizontal rows of pits in severe cases, or absence of enamel in extreme cases. (12 Dec 1998) |
| optic nerve hypoplasia | Congenitally small optic disk resulting from failure of development of retinal ganglion cells, with a reduced number of axons; visual impairment may be marked. See: de Morsier's syndrome. (05 Mar 2000) |
| thymic hypoplasia | diGeorge syndrome |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|