| Crouzon, Octave | <person> French physician, 1874-1938. See: Crouzon's disease, Crouzon's syndrome. (05 Mar 2000) |
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| crouzon's disease | <disease> A genetic disorder (autosomal dominant) characterised by abnormalities of the cranial sutures, widening of the skull, a high forehead, ocular hypertelorism, exophthalmos, beaked nose and hypoplasia of the maxilla Inheritance: autosomal dominant. (27 Sep 1997) |
| Crouzon's syndrome | <paediatrics> A genetic disorder (autosomal dominant) characterised by abnormalities of the cranial sutures, widening of the skull, a high forehead, ocular hypertelorism, exophthalmos, beaked nose and hypoplasia of the maxilla Inheritance: autosomal dominant. (27 Sep 1997) |
| crouzon syndrome | <radiology> Craniofacial dysostosis, autosomal dominant, premature closure of sutures, usually coronal most likely to be brachycephaly, all sutures most likely to be Kleeblatschaedel, hypoplasia of facial bones, beaked (parrot) nose (12 Dec 1998) |
| Crouzon's d. |
craniofacial dysostosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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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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