| CS | calf serum; campomelic syndrome; carcinoid syndrome; cardiogenic shock; caries-susceptible; carotid ... |
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| EBDCT | Cockayne-Touraine type of epidermolysis bullosa dystrophica |
| Cockayne | Edward A., British physician, 1880-1956. See: Cockayne's disease, Cockayne's syndrome, Weber-Cockayne syndrome. (05 Mar 2000) |
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| cockayne syndrome | <radiology> Type of dysmyelinating disease, autosomal recessive, onset usually within 2nd year, (?) variant of Pelizaeus-Merzbacher disease, distinguish from Kearns-Sayre syndrome CT findings: microcephaly, basal ganglion calcification, cerebral atrophy (12 Dec 1998) |
| Cockayne's disease | <syndrome> Dwarfism, precociously senile appearance, pigmentary degeneration of the retina, optic atrophy, deafness, sensitivity to sunlight, and mental retardation; autosomal recessive inheritance. There is a variant with early onset. Synonym: Cockayne's disease. (05 Mar 2000) |
| Cockayne's syndrome | <syndrome> Dwarfism, precociously senile appearance, pigmentary degeneration of the retina, optic atrophy, deafness, sensitivity to sunlight, and mental retardation; autosomal recessive inheritance. There is a variant with early onset. Synonym: Cockayne's disease. (05 Mar 2000) |
| Weber-Cockayne syndrome | <syndrome> This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
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Synonyms : Cockayne Syndrome, Group A, Cockayne Syndrome, Group B, Cockayne Syndrome, Group C, Cockayne Syndrome, Type A, Cockayne Syndrome, Type B, Cockayne Syndrome, Type C, Cockayne Syndrome, Type I, Cockayne Syndrome, Type II, Cockayne Syndrome, Type III
| Cockayne syndrome |
A genetic condition characterized by short stature, premature aging, sensitivity to light, and possibly deafness and mental retardation.
출처: www.seniormag.com/conditions/cancer/cancerglossary...
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| Cockayne syndrome |
Rare inherited disorder characterized by growth retardation, mental retardation, retinal atrophy, abnormal sensitivity to light, and progressive sensorineural hearing loss of later onset
출처: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Cockayne's s. |
a hereditary syndrome transmitted as an autosomal recessive trait, consisting of dwarfism with retinal atrophy and deafness, associated with progeria, prognathism, mental retardation, and photosensitivity.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Cockayne's syndrome |
see under syndrome.
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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