| HSD | Hallervorden-Spatz disease; honestly significant difference; hydroxysteroid dehydrogenase; hypertoni... |
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| HSS | Hallermann-Streiff syndrome; Hallervorden-Spatz syndrome; Henoch-Schonlein syndrome; high-speed supe... |
| HSD | Hallervorden Spatz disease |
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| HSS | Hallervorden Spatz syndrome |
| Spatz, Hugo | <person> German neurologist and psychiatrist, 1888-1969. See: Hallervorden-Spatz disease, Hallervorden-Spatz syndrome. (05 Mar 2000) |
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| Hallervorden-Spatz syndrome | <neurology, syndrome> A progressive hereditary disorder with marked reduction in the number of myelin sheaths of the globus pallidus and substantia nigra with accumulation of iron pigment. Manifestations include dysarthria, progressive mental deterioration, and corticospinal and extrapyramidal motor signs. CT findings: high-signal lesions in globus pallidus bilaterally. MRI findings: (T2-weighted spin-echo), hypointensity in globus pallidus (iron accumulation), small area of hyperintensity in internal segment (so-called eye of the tiger sign) corresponding to area of gliosis and vacuolation. Inheritance: autosomal recessive. (20 Mar 2000) |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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