Cowden's syndrome. Case report, with reference to an affected family;Síndrome de Cowden. A propósito de una familia afectada

Medicina Oral, Patologia Oral y Cirugia Bucal

Volumn 11, Issue 1, 2006, Pages 12-16

  Blanco, Verónica ^a,b,d   Keochgerián, Verónica ^c,d  

^a Cátedra de Semiología y Patología Buco Maxilo Facial   (Uruguay)

^b Servicio de Urgencia   (Uruguay)

^c Cátedra de Anatomía Patológica

^d UNIVERSIDAD DE LA REPÚBLICA   (Uruguay)

Author keywords

Multiple hamartomas; Preneoplasic; Syndrome; Tumour suppressor gen

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PTEN PROTEIN, HUMAN;

ADULT; ARTICLE; BREAST LESION; CANCER GROWTH; CANCER STAGING; CANCER SUSCEPTIBILITY; CASE REPORT; CLINICAL FEATURE; COWDEN SYNDROME; DNA MODIFICATION; GENE MUTATION; GENODERMATOSIS; HAMARTOMA; HUMAN; INTESTINE POLYP; MALE; MEDICAL EXAMINATION; PHENOTYPE; PROTEIN EXPRESSION; THYROID DISEASE; TUMOR BIOPSY; TUMOR SUPPRESSOR GENE; UROGENITAL TRACT DISEASE; CONGENITAL TUMOR; FAMILY HEALTH; GENETICS; MIDDLE AGED; MOUTH MUCOSA; MOUTH TUMOR; PAPILLOMA; PATHOLOGY;

ADULT; FAMILY HEALTH; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; INTESTINAL POLYPS; MALE; MIDDLE AGED; MOUTH MUCOSA; MOUTH NEOPLASMS; PAPILLOMA; PTEN PHOSPHOHYDROLASE;

EID: 33644788771     PISSN: 16984447     EISSN: 16986946     Source Type: Journal    
DOI: None     Document Type: Article

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