| HGPS | hereditary giant platelet syndrome; Hutchinson-Gilford progeria syndrome |
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| progeria | <syndrome> Accelerated aging syndrome in which most of the characteristic stages of human senescence are compressed into less than a decade. Defect probably in DNA repair. (18 Nov 1997) |
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| progeria with cataract | A syndrome of bony anomalies of the calvaria, face, and jaw, with brachygnathia, narrow curved nose, and multiple ocular defects including microphthalmia, microcornea, and cataract, often with alopecia overlying skull sutures, or alopecia areata and hypoplasia, or absence of eyebrows. The pattern of inheritance is undecided. Synonym: congenital sutural alopecia, Hallermann-Streiff syndrome, Hallermann-Streiff-Francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial syndrome, progeria with cataract, progeria with microphthalmia. (05 Mar 2000) |
Synonyms : Hutchinson Gilford Syndrome, Syndrome, Hutchinson-Gilford
| progeria |
a rare abnormality marked by premature aging (grey hair and wrinkled skin and stooped posture) in a child
출처: wordnet.princeton.edu/perl/webwn
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| progeria |
A human disease or syndrome in which some characteristics of senescence are accelerated so that relatively young individuals appear prematurely aged. Examples include Hutchinson Guilford Syndrome (HGS is a rare autosomal-dominant disorder with a classic withered presentation leading to an early death in the teenage years. ...
출처: images.antiagingconference.com/files/1103/aagatewa...
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| progeria | a rare abnormality marked by premature aging (gray hair and wrinkled skin and stooped posture) in a child |
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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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