Results 11 to 20 of about 2,571 (160)
Involution of mucocutaneous pigmentation of the Peutz-Jeghers syndrome. [PDF]
BMJ: British Medical Journal, 1977 P W Keeling
exaly +3 more sources
Indian Journal of Dental Research, 2023 Introduction: Patients with end-stage renal disease (ESRD) suffer from mucocutaneous changes that could significantly impair the quality of life. We aimed this study to assess the mucocutaneous changes in hemodialysis patients and to correlate the serum ...
Asmaa A. Ras +4 more
doaj +1 more source
Peutz-Jeghers syndrome in pediatric patients: experience in a tertiary care institution in Mexico
Boletín Médico del Hospital Infantil de México, 2022 Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease characterized by the development of polyps in the gastrointestinal tract, mucocutaneous pigmentation, and the risk of developing malignant neoplasms. This study aimed
Rodrigo Ortegón-Gallareta +7 more
doaj +1 more source
Solitary Peutz-Jeghers Polyp of Jejunum with Dysplasia Presenting as Intussusception [PDF]
National Journal of Laboratory Medicine, 2015 Peutz-Jeghers syndrome is inherited as an autosomal dominant disorder presenting as hamartomatous polyps in small bowel with mucocutaneous pigmentation.
Deepti Agarwal +3 more
doaj +1 more source
Respiratory Medicine Case Reports, 2023 Dyskeratosis congenita is a rare genetic disorder of telomere insufficiency characterized by a mucocutaneous triad of nail dystrophy, abnormal skin pigmentation, and mucosal leukoplakia.
Jinhee Han, Jin Woo Song
doaj +1 more source
Clinical periodontal diagnosis
Periodontology 2000, EarlyView., 2023 Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi +5 more
wiley +1 more source
Family with Peutz–Jeghers syndrome in Indonesia
JGH Open, 2022 Peutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterised by mucocutaneous pigmentation, gastrointestinal polyps and an increased risk of gastrointestinal and other cancers.
Muhammad Luthfi Parewangi +9 more
doaj +1 more source
A case of labial lentigines in Peutz-Jeghers syndrome treated using a Q-switched alexandrite laser
Chinese Journal of Plastic and Reconstructive Surgery, 2021 Peutz-Jeghers syndrome (PJS) is a polygenic autosomal dominant disease characterized by multiple gastrointestinal polyps and pigmentation of the mucosa and skin.
Shuai Yang +4 more
doaj +1 more source
The importance of early diagnosis and surveillance in Peutz-Jeghers Syndrome: A case report
Acta Marisiensis - Seria Medica, 2023 Introduction: Peutz-Jeghers syndrome is a rare autosomal dominant inherited disorder characterized by hamartomatous intestinal polyps and mucocutaneous pigmentation. Most cases appear to be linked to the mutation of the STK11 gene.
Balosin Marina-Georgia
doaj +1 more source
Peutz-Jeghers syndrome: A case report
Asian Journal of Medical Sciences, 2021 Peutz-jeghers syndrome is a rare inherited autosomal dominant disease which is characterized by mucocutaneous pigmentation and multiple polyps in the gastrointestinal tract.
Pratima Poudel , Roushan Jahan
doaj +1 more source