| WD | wallerian degeneration; well developed; well differentiated; wet dressing; Whitney Damon [dextrose];... |
|---|
| WD | Wolman disease |
|---|
| wolman disease | <radiology> Rare, familial xanthomatosis, causes death early in infancy, adrenal calcification, diffuse, punctate calcifications throughout, enlarged, normally shaped adrenals, hepatosplenomegaly (12 Dec 1998) |
|---|---|
| Wolman's disease | See: cholesterol ester storage disease. Compare: cholesterol ester storage disease. (05 Mar 2000) |
| Wolman's xanthomatosis | A rare benign adult form of inherited lysosomal lipid storage disease that is due to deficiency of acid lipase. It results in an accumulation of neutral lipids, particularly cholesterol esters, within cells (particularly leukocytes, fibroblasts, and liver cells). It is an allelic variant of wolman disease. (12 Dec 1998) |
| Wolman, Moshe | <person> 20th century Israeli neuropathologist, *1914. See: Wolman's disease, Wolman's xanthomatosis. (05 Mar 2000) |
Synonyms : Liposomal Acid Lipase Deficiency, Wolman Type, Wolman's Disease, Disease, Wolman, Disease, Wolman's, Familial Xanthomatoses, Familial Xanthomatosis, Wolman's Xanthomatosis, Wolmans Disease, Xanthomatoses, Familial, Xanthomatosis, Wolman, Xanthomatosis, Wolmans
| Wolman's disease |
Wolman's disease or Wolman’s syndrom is a rare (named after Moshe Wolman) , inborn metabolic disorder (lipidosis) in which infants develop hepatosplenomegaly, calcification of the adrenal glands, and foam cells in the bone marrow and other tissues. Inclusion bodies of lipid droplets can be seen in the circulating white cells. After a few weeks when the child is mentally bright and alert it manifests in the first few weeks of life with failure to thrive, diarrhoea, vomiting. ...
출처: en.wikipedia.org/wiki/Wolman's_disease
|
|---|---|
| Wolman disease |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| Wolman's d. |
a lysosomal storage disease caused by deficiency of the lysosomal sterol esterase, with onset in early infancy and death before one year of age. Clinical features include hepatosplenomegaly, steatorrhea, abdominal distension, anemia, inanition, and adrenal calcification. Called also primary familial or Wolman xanthomatosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|