| 영문 | ovary | 한글 | 난소 |
|---|---|---|---|
| 설명 | 여성의 성기관으로 수정에 필요한 난자를 만든다. 자궁의 주위 양쪽으로 2개가 있으며, 여성호르몬을 생성하여 여성으로서의 2차성징 발달에 기여한다. 난소에 생성된 난자는 난관에서 수정이 되거나, 혹은 수정이 되지 않은 채, 자궁관을 따라 자궁에 이르게 되고 이후 황체기를 맞이한 난소에서 나오는 황체호르몬에 의해 월경이 시작된다(수정이 되면, 난소에서는 황체의 형성이 일어나지 않으며, 월경이 발생하지 않고 임신을 유지하게 된다). 난소에서는 호르몬의 자극으로 난자를 생성하게 된다. 또한 이것은 월경의 형성과 밀접한 관계가 있다. 여성의 월경은 정해준 순서에 의해 일어나게 된다. 먼저 난포자극호르몬(FSH)이 뇌에서 분비되어 여성의 난소를 자극하게 되면 난포가 자극받아 난포호르몬을 분비하게 되고 이것은 다시 되먹이기 기전에 의해 뇌에 작용을 하여 황체화호르몬이 뇌에서 분비되고 이것이 이른바 절정(다른 말로 이것을 LH 절정이라고 부른다)에 이르렀을 때, 난포에서 배란(난자가 난소밖으로 나가는 현상)이 일어나게 된다. 이후 난포는 황체로 변하게 되며, 배란된 난자가 수정되지 아니하면, 황체는 황체호르몬(프로제스테론, progesteron)을 분비한뒤 퇴화되고 곧이어 월경이 일어나게 된다. 이 일은 정상적인 대부분의 여성에서 28일을 주기로 일어나며, 대개 LH 절정이후 마지막은 14일로 일정하다고 한다. |
||
| OPCOS | oligomenorrheic polycystic ovary syndrome |
|---|---|
| PCO | patient complains of; polycystic ovary; predicted cardiac output |
| PCOS | polycystic ovary syndrome |
| POD | peroxidase; place of death; podiatry; polycystic ovary disease; pool of doctors; postoperative day; ... |
| POS | periosteal osteosarcoma; physician order set; point of service; polycystic ovary syndrome; psychoorg... |
| PCOS | PolyCystic Ovary Syndrome |
|---|---|
| PCOD | Polycystic Ovary Disease |
| PCO | Polycystic Ovary Syndrome |
| PCO | Polycystic ovary |
| CHO | 3-Chinese hamster ovary |
| polycystic ovary | Enlarged cystic ovary's, pearl white in colour, with thickened tunica albuginea, characteristic of the Stein-Leventhal syndrome; clinical features are abnormal menses, obesity, and evidence of masculinization, such as hirsutism. (05 Mar 2000) |
|---|---|
| polycystic ovary syndrome | <syndrome> Clinical symptom complex characterised by oligomenorrhoea or amenorrhoea, anovulation, and regularly associated with bilateral polycystic ovaries. (12 Dec 1998) |
| polycystic | Composed of many cysts. (05 Mar 2000) |
| polycystic disease of kidneys | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
| polycystic kidney | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
| polycystic kidney disease | <disease> A rare inherited condition in which the kidney are composed of multiple cysts. Kidney cysts are associated with an increased incidence of cerebral aneurysm. Symptoms usually appear later (if they do at all) and include blood in the urine, flank pain, excessive urination at night and abdominal pain. Individuals may also have elevated blood pressure. Chronic (end-stage renal disease) renal failure is the most common result in the 5th to 6th decades of life. Incidence: 1 in 5,000. (02 Jan 1998) |
| polycystic liver | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic liver disease | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic ovarian disease | <disease> A condition found among women who do not ovulate, characterised by multiple ovarian cysts and increased androgen production. (09 Oct 1997) |
| disease, ovarian, polycystic | See Disease, polycystic ovarian. (12 Dec 1998) |
| disease, polycystic kidney | Genetic (inherited) disorders characterised by the development of innumerable cysts in the kidneys filled with fluid that replace much of the mass of the kidneys and reduce kidney function leading to kidney failure. (12 Dec 1998) |
| disease, polycystic ovarian | An hormonal problem that causes women to have a variety of symptoms including irregular or no periods, acne, obesity and excessive hair growth. Women with PCO are at a higher risk for uterine cancer (endometrial cancer), diabetes, high blood pressure, and heart disease. With proper treatment, risks can be minimised. PCO is also known as Stein-Leventhal syndrome. (12 Dec 1998) |
| kidney, polycystic | Kidney whose tissue is displaced by a large number of tightly packed cysts so that cystic volume predominates over the solid parts to a considerable degree. (12 Dec 1998) |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|