poikiloderma congenitale

Roth·mund syn·drome

(rot'mūnd), atrophy, pigmentation, and telangiectasia of the skin, usually with juvenile cataract, saddle nose, congenital bone defects, disturbance of hair growth, hypogonadism; autosomal recessive inheritance. Synonym(s): poikiloderma atrophicans and cataract, poikiloderma congenitale, Rothmund-Thomson syndrome

Rothmund,

August von, German physician, 1830-1906. Rothmund syndrome - atrophy, pigmentation, and telangiectasia of the skin, usually with juvenile cataract, saddle nose, congenital bone defects, disturbance of hair growth and hypogonadism. Synonym(s): poikiloderma atrophicans and cataract; poikiloderma congenitale; Rothmund-Thomson syndromeRothmund-Thomson syndrome - Synonym(s): Rothmund syndrome

单词	poikiloderma congenitale
释义	poikiloderma congenitale Roth·mund syn·drome (rot'mūnd), atrophy, pigmentation, and telangiectasia of the skin, usually with juvenile cataract, saddle nose, congenital bone defects, disturbance of hair growth, hypogonadism; autosomal recessive inheritance. Synonym(s): poikiloderma atrophicans and cataract, poikiloderma congenitale, Rothmund-Thomson syndrome Rothmund, August von, German physician, 1830-1906. Rothmund syndrome - atrophy, pigmentation, and telangiectasia of the skin, usually with juvenile cataract, saddle nose, congenital bone defects, disturbance of hair growth and hypogonadism. Synonym(s): poikiloderma atrophicans and cataract; poikiloderma congenitale; Rothmund-Thomson syndromeRothmund-Thomson syndrome - Synonym(s): Rothmund syndrome
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