| CDP | chondrodysplasia punctata; chronic destructive periodontitis; collagenase-digestible protein; contin... |
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| CDPR | chondrodysplasia punctata, rhizomelic |
| CDPX | X-linked chondrodysplasia punctata |
| CP | candle power; capillary pressure; cardiac pacing; cardiac performance; cardiopulmonary; caudate puta... |
| CPXD | chondrodysplasia punctata, X-linked dominant |
| RCDP | Rhizomelic Chondrodysplasia Punctata |
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| chondrodysplasia | <embryology, orthopaedics> A disturbance in the development of cartilage, primarily the long bones. This can result in arrested growth and dwarfism. Origin: Gr. Plassein = to form (15 Jan 1998) |
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| chondrodysplasia punctata | A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. (12 Dec 1998) |
| chondrodysplasia punctata, rhizomelic | An autosomal recessive form of chondrodysplasia punctata characterised by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondrial bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|