- Cowden disease
- Cow·den disease (kouґdən) [Cowden, the family name of the first reported case] see under disease.
Medical dictionary. 2011.
Cowden disease
Look at other dictionaries:
Cowden disease — Germ line mutations in PTEN are responsible for Cowden disease, a rare autosomal dominant multiple hamartoma syndrome … Dictionary of molecular biology
Cowden disease — an autosomal dominant disorder caused by a mutation on chromosome 10q, comprising a combination of ectodermal, mesodermal, and endodermal anomalies; it is characterized by development of multiple hamartomatous lesions, especially in the skin,… … Medical dictionary
Cowden-Syndrom — Das Cowden Syndrom, das im Englischen auch als Cowden disease oder multiple hamartoma syndrome bezeichnet wird, ist ein pleomorphes, autosomal dominant auftretendes Syndrom, das klinisch durch Hamartome aller drei Keimblätter in Erscheinung tritt … Deutsch Wikipedia
Cowden syndrome — Classification and external resources hamartomas papules on the area around the nose of a patient with Cowden syndrome ICD 9 … Wikipedia
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Cowden — Surname of the family from which the condition subsequently known as C. disease was first reported … Medical dictionary
Lhermitte-Duclos disease — Infobox Disease Name = Lhermitte Duclos disease Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 158350 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = | MeshID = D006223 Lhermitte Duclos disease (dysplastic gangliocytoma of… … Wikipedia
Maladie de Cowden — Syndrome de Cowden Syndrome de Cowden Autre nom Maladie de Cowden Référence MIM … Wikipédia en Français
Syndrome de cowden — Autre nom Maladie de Cowden Référence MIM … Wikipédia en Français
Syndrome de Cowden — Référence MIM 158350 Transmission Dominante Chromosome 10q23.31 Gène PTEN Empreinte parentale Non … Wikipédia en Français
