| ¿µ¹® | puberty | ÇÑ±Û | »çÃá±â |
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| PP | diphosphate group; emphysema [pink puffers]; near point of accommodation [Lat. punctum proximum]; pa... |
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| IPH | idiopathic portal hypertension; idiopathic pulmonary hemosiderosis; idiopathic pulmonary hypertensio... |
| OAP | Office of Adolescent Pregnancy; old age pension, old age pensioner; ophthalmic artery pressure; oste... |
| IHSS(= HCMP) | Idiopathic Hypertrophic Subaortic Stenosis = Obstructive Idiopathic Hypertrophic Car... |
| DISH | diffuse idiopathic skeletal hyperostosis; disseminated idiopathic skeletal hyperostosis |
| CPP | Central precocious puberty |
|---|---|
| PP | Precocious puberty |
| PP | Precocious pubarche |
| CDGP | Constitutional delay of growth and puberty |
| ICP | infancy childhood puberty |
| precocious puberty | Condition in which pubertal changes begin at an unexpectedly early age; often the result of a pathological process involving a gland capable of secreting oestrogens or androgens, e.g., the ovary or the adrenal cortex. Synonym: pubertas praecox. (05 Mar 2000) |
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| puberty, precocious | Unusually early sexual maturity. (12 Dec 1998) |
| precocious | 1. Ripe or mature before the proper or natural time; early or prematurely ripe or developed; as, precocious trees. 2. Developed more than is natural or usual at a given age; exceeding what is to be expected of one's years; too forward; used especially of mental forwardness; as, a precocious child; precocious talents. Origin: L. Praecox, -ocis, and praecoquus, fr. Praecoquere to cook or ripen beforehand; prae = before + coquere to cook. See Cook, and cf. Apricot. Source: Websters Dictionary (01 Mar 1998) |
| puberty | <paediatrics> The period during which the secondary sex characteristics begin to develop and the capability of sexual reproduction is attained. Origin: L. Pubertas (18 Nov 1997) |
| puberty, delayed | Unusually late sexual maturity. (12 Dec 1998) |
| acute idiopathic polyneuritis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| chronic idiopathic jaundice | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
| chronic idiopathic xanthomatosis | Vague or indefinite term for inherited abnormalities of lipid metabolism leading to xanthoma formation (e.g., primary familial xanthomatosis). (05 Mar 2000) |
| multiple idiopathic haemorrhagic sarcoma | <oncology, tumour> A type of vascular cancer characterised by soft purple nodules that usually develop first on the feet and then slowly spread across the skin.This cancer is most often found in people with compromised immune systems, such as AIDS patients. (09 Oct 1997) |
| primary idiopathic macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| purpura, thrombocytopenic, idiopathic | Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IgG autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. (12 Dec 1998) |
| hyperostosis, diffuse idiopathic skeletal | A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions. (12 Dec 1998) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| idiopathic | Of the nature of an idiopathy, self originated, of unknown causation. (18 Nov 1997) |
| idiopathic aldosteronism | An adrenocortical disorder caused by excessive secretion of aldosterone and characterised by headaches, nocturia, polyuria, fatigue, hypertension, potassium depletion, hypokalaemic alkalosis, hypervolaemia, and decreased plasma renin activity; may be associated with small benign adrenocortical adenomas. Synonym: Conn's syndrome, idiopathic aldosteronism. (05 Mar 2000) |
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