Gardner syndrome (Q46681): Difference between revisions

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Síndrome de Gardner desenvolve pólipos adenomatosos em todo o trato gastrointestinal, acompanhados por manifestações extracolônicas, incluindo adenomas periampulares, carcinoma papilar da tireoide, hepatoblastoma, osteomas de mandíbula e crânio, cistos epidérmicos e tumores desmoides. Síndrome de Gardner é um termo usado para se referir a pacientes nos quais essas características extraintestinais são excepcionalmente proeminentes.
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Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, hepatoblastoma, osteomas of the mandible and skull, epidermal cysts, and desmoid tumours. Gardner syndrome is a term used to refer to patients in whom these extraintestinal features are unusually prominent.

Revision as of 15:26, 13 August 2026

Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, hepatoblastoma, osteomas of the mandible and skull, epidermal cysts, and desmoid tumours. Gardner syndrome is a term used to refer to patients in whom these extraintestinal features are unusually prominent.
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    English
    Gardner syndrome
    Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, hepatoblastoma, osteomas of the mandible and skull, epidermal cysts, and desmoid tumours. Gardner syndrome is a term used to refer to patients in whom these extraintestinal features are unusually prominent.

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