| 영문 | cyanosis | 한글 | 청색증 |
|---|---|---|---|
| 설명 | 피부나 점막이 푸르스름해지는 것으로 환원 적혈구가 많을 경우에 나타난다. 적혈구속에 산소와 결합하여 산소를 운반하는 역할을 하는 것을 혈색소라고 하는데 이 혈색소가 산소와 결합하지 못한 것을 환원 혈색소라고 한다. 대개 이 환원적혈구의 혈중농도가 5%이상일 경우에 청색증이 나타난다. 이 청색증은 특히, 입술, 손가락의 끝, 귀 등에서 쉽게 관찰이 되어진다. 이 청색증은 중심성과 말초성의 두 가지로 나뉘어질 수가 있다. 중심성 청색증(central cyanosis)은 혀, 입술, 구강점막 등 중심부위에 주로 청색증이 나타나는 경우로 이 경우는 폐에서 가스교환의 문제가 있어서 동맥혈에 일정량 이하의 산소가 포함이 되어 있는 경우에 생기는 현상으로 호흡기 질환이나, 해발 2400미터이상의 고지에 있는 경우에 생길 수가 있다. 말초성 청색증(peripheral cyanosis)은 손가락 등의 신체의 말단 부위에 청색증이 있는 경우로 주로 혈류의 순환의 이상으로 혈류가 신체의 말초에 지체되어 있는 경우에 주로 발생한다. |
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| ABC | absolute basophil count; absolute bone conduction; acalculous biliary colic; acid balance control; a... |
|---|---|
| CCE | carboline carboxylic acid ester; chamois contagious ecthyma; clear-cell endothelioma; clubbing, cyan... |
| CN | caudate nucleus; cellulose nitrate; charge nurse; child nutrition; chloroacetophenone; clinical nurs... |
| cy, cyan | cyanosis |
| AHC | Albright's Hereditary Osteodystrophy |
| AHO | Albright hereditary osteodystrophy |
|---|---|
| CHED | Congenital Hereditary Endothelial Dystrophy |
| HANE | Hereditary Angio Neurotic Edema |
| HAE | Hereditary Angio-Edema |
| HCSMA | Hereditary Canine Spinal Muscular Atrophy |
| hereditary methemoglobinaemic cyanosis | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
|---|---|
| cyanosis | <clinical sign> A bluish discolouration, applied especially to such discolouration of skin and mucous membranes due to excessive concentration of reduced haemoglobin in the blood. Origin: Gr. Kyanos = blue (21 May 1997) |
| cyanosis retinae | Venous congestion of the retina. Shunt cyanosis, any blue colour of the entire skin or a region of the skin or mucous membrane due to a right to left shunt permitting unoxygenated blood to reach the left side of the circulation. (05 Mar 2000) |
| tardive cyanosis | cyanose tardive |
| toxic cyanosis | Cyanosis due to methemoglobin formation resulting from the action of certain drugs, e.g., nitrites. (05 Mar 2000) |
| late cyanosis | cyanose tardive |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |
| hereditary amyloidosis | <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur. Inheritance: autosomal dominant. Synonym: familial amyloidosis, hereditary amyloidosis. (05 Mar 2000) |
| hereditary angioedema | A genetic form of angioedema. (angioedema is also referred to as quinke's disease.) persons with it are born lacking an inhibitor protein (called c1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of c1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|