Search results for "Hamartomatosos"

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Register and clinical follow-up of patients with Peutz-Jeghers syndrome in Valencia

2020

Introduction and aims: Peutz-Jeghers syndrome is a rare autosomal dominant inherited disease caused by a germline mutation of the STK11/LKB1 gene, located on chromosome 19p13.3. It is characterized by mucocutaneous hyperpigmentation, hamartomatous polyposis, and predisposition to cancer. The aim of the present study was to identify and register patients with Peutz-Jeghers syndrome, describe the disease, and estimate its prevalence in Valencia (Spain). Materials and methods: A print-out of the clinical histories from 10 hospitals was obtained utilizing the ICD-9 code 759.6 from the Minimum Basic Data Set of Hospital Admissions of the Spanish Ministry of Health and Consumer Affairs. Results: …

Pediatricsmedicine.medical_specialtyAnemiaMucocutaneous zonePrevalencePeutz–Jeghers syndromeDisease03 medical and health sciences0302 clinical medicineCáncer hereditariomedicine030212 general & internal medicinePóliposlcsh:RC799-869business.industrySTK11CancerInvaginationGeneral Medicinemedicine.diseaseBowel obstructionHamartomatosos030228 respiratory systemlcsh:Diseases of the digestive system. GastroenterologybusinessPeutz JeghersRevista de Gastroenterología de México (English Edition)
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