A novel mutation of PTEN gene in a patient with Cowden syndrome with excessive papillomatosis of the lips, discrete cutaneous lesions, and gastrointestinal polyposis

European Journal of Gastroenterology and Hepatology

Volumn 19, Issue 6, 2007, Pages 513-517

  Vasovcak, Peter ^a   Krepelova, Anna ^a   Puchmajerova, Alena ^a   Spicak, Julius ^b   Voska, Ludek ^b   Musilova, Andrea ^b   Mestak, Jan ^b   Martinek, Jan ^b,c  

^a UNIVERSITY HOSPITAL MOTOL   (Czech Republic)

^b UNIVERSITY HOSPITAL BULOVKA   (Czech Republic)

^c INSTITUTE FOR CLINICAL AND EXPERIMENTAL MEDICINE   (Czech Republic)

Author keywords

Cowden syndrome; Hamartomatous polyps; Mucocutaneous lesions; Peutz Jeghers syndrome

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ACANTHOSIS; ADULT; ARTICLE; CASE REPORT; COLON POLYP; COWDEN SYNDROME; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DUODENUM POLYP; ESOPHAGUS DISEASE; GASTROINTESTINAL POLYPOSIS; GENE DELETION; GENETIC SCREENING; HUMAN; LIP TUMOR; MALE; MEDICAL EXAMINATION; MUSCLE SPASM; MUTATIONAL ANALYSIS; PAPILLOMATOSIS; PEUTZ JEGHERS SYNDROME; PLASTIC SURGERY; PRIORITY JOURNAL; RECTUM POLYP; RELIABILITY; SKIN MANIFESTATION; STOMACH POLYPOSIS; TRACHEA DISEASE; TREATMENT OUTCOME;

ADULT; GENE DELETION; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; INTESTINAL POLYPOSIS; LIP NEOPLASMS; MALE; PAPILLOMA; PTEN PHOSPHOHYDROLASE; SKIN;

EID: 34248197032     PISSN: 0954691X     EISSN: None     Source Type: Journal    
DOI: 10.1097/MEG.0b013e3280d6ed4b     Document Type: Article

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