Kohlmeier-Degos syndrome

Kohl·mei·er-De·gos syn·drome

(kōl'mī-ĕr dā-gō'), vascular occlusive disorder predominantly involving the small arteries of the skin and bowel with about one fifth of patients having central nervous system symptoms secondary to arterial fibrosis and thrombosis.

Degos,

Robert, French dermatologist, 1904-1987. Degos acanthoma - obsolete term for clear cell acanthoma.Degos disease - a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules followed by peritonitis, progressive neurological disability, and death. Synonym(s): Degos syndrome; malignant atrophic papulosisDegos syndrome - Synonym(s): Degos diseaseKohlmeier-Degos syndrome - see under Kohlmeier

Kohlmeier,

W., German physician. Kohlmeier-Degos syndrome - vascular occlusive disorder predominantly involving the small arteries of the skin and bowel.

单词	kohlmeier-degos syndrome
释义	Kohlmeier-Degos syndrome Kohl·mei·er-De·gos syn·drome (kōl'mī-ĕr dā-gō'), vascular occlusive disorder predominantly involving the small arteries of the skin and bowel with about one fifth of patients having central nervous system symptoms secondary to arterial fibrosis and thrombosis. Degos, Robert, French dermatologist, 1904-1987. Degos acanthoma - obsolete term for clear cell acanthoma.Degos disease - a cutaneovisceral syndrome characterized by pathognomonic umbilicated porcelain-white papules followed by peritonitis, progressive neurological disability, and death. Synonym(s): Degos syndrome; malignant atrophic papulosisDegos syndrome - Synonym(s): Degos diseaseKohlmeier-Degos syndrome - see under Kohlmeier Kohlmeier, W., German physician. Kohlmeier-Degos syndrome - vascular occlusive disorder predominantly involving the small arteries of the skin and bowel.
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