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单词 gardner syndrome
释义 DictionarySeeGardner's syndrome

Gardner syndrome


Gard·ner syn·drome

(gard'nĕr), [MIM*175100-0006] multiple polyposis predisposing to carcinoma of the colon; also multiple tumors, osteomas of the skull, epidermoid cysts, and fibromas; autosomal dominant inheritance, caused by mutation in the adenomatous polyposis coli gene (APC) on chromosome 5q. This disorder is allelic to familial adenomatous polyposis (FAP).

Gardner syndrome

Genetics An AD condition characterized by multiple–100s to 1000s of premalignant polyps of the large intestine; carcinoma may develop in the teens in the Pts

Gard·ner syn·drome

(gahrd'nĕr sin'drōm) Multiple polyposis predisposing to carcinoma of the colon; also multiple tumors, osteomas of the skull, epidermoid cysts, and fibromas; autosomal dominant inheritance, caused by mutation in the adenomatous polyposis coli gene (APC) on chromosome 5q. This disorder is allelic to familial adenomatous polyposis.

Gardner,

Eldon John, U.S. geneticist, 1909-1987. Fitzgerald-Gardner syndrome - see under FitzgeraldGardner syndrome - multiple polyposis predisposing to carcinoma of the colon.

Gardner,

W.J., U.S. physician. Gardner syndrome - bilateral acoustic nerve neuromas resulting in progressive loss of hearing and neurologic complications; may result in tumors of the brain, colon, skin, pancreas, skeleton, thyroid, or mandible.

Gard·ner syn·drome

(gahrd'nĕr sin'drōm) [MIM*175100-0006] Multiple polyposis predisposing to carcinoma of the colon.
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