Results 111 to 120 of about 402,657 (223)

Familial pediatric Peutz–Jeghers syndrome with recurrent intussusception: case report and literature review

Frontiers in Pediatrics
BackgroundPeutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis, predisposing affected individuals to recurrent small bowel intussusception and ...
Sondes Sahli, Sondes Sahli, Bochra Aziza, Bochra Aziza, Nada Sghairoun, Nada Sghairoun, Asma Slimani, Asma Slimani, Nadia Boujelbene, Nadia Boujelbene, Nadia Boujelbene, Rim Missaoui, Rim Missaoui, Rim Missaoui, Zohra Rahal, Zohra Rahal, Said Jlidi, Said Jlidi   +17 more
doaj   +1 more source

Cronkhite- Canada Syndrome

Indian Journal of Dermatology, 1997
A case of Cronkhite- Canada syndrome in a 59 year old male is reported. The patient presented with generalized hyper pigmentation, alopecia, loss of finger and toenails, diarrhoea, weight loss and gastro- intestinal polyposis.
Narendra, Shenoy S D, Bejoy P, Srinivas C R   +3 more
doaj  

Schistosoma Mansoni and Haematobium: Radiological Diagnostic Clues and Pathophysiology

Pathogens
Schistosomiasis (bilharzia) is a parasitic infection caused by trematodes of the Schistosoma genus and remains a significant health burden in endemic regions. Granulomatous host responses to deposited Schistosoma eggs in small veins and tissues result in
Sultan Abdulwadoud Alshoabi, Abdullatif O. Magram, Abdulaziz H. Alkalady, Rafat Rashed Al-Maqtari, Khaled M. Almas, Khaled Mohammed Al-Sayaghi, Abdullgabbar M. Hamid, Fahad H. Alhazmi, Abdulaziz A. Qurashi, Walaa Alsharif, Amirah Alsaedi, Ezzat AbuAzzah, Abdulkareem Algahtani, Khaled A. Alqfail, Khalid M. Alshamrani   +14 more
doaj   +1 more source

Familial intestinal polyposis

Journal of British Surgery, 1966
D H, Thompson, W M, Roberts, J C, Comline   +2 more
openaire   +2 more sources

Human intestinal spirochetes are distinct from Serpulina hyodysenteriae [PDF]

, 1993
Twenty-nine intestinal spirochetes isolated from Australian aboriginal children and six strains from Italian adults (HRM1, -2, -4, -5, -7, and -14) were genetically examined at 15 enzyme loci by using multilocus enzyme electrophoresis.
Lymbery, A.J., Hampson, D.J., McLaren, A.J., Lee, J.I.   +3 more
core  

Small Intestinal Polyposis [PDF]

Proceedings of the Royal Society of Medicine, 1959
openaire   +2 more sources

Proctocolectomy and ileal J-pouch anal anastomosis on the surgical treatment of familial adenomatous polyposis and ulcerative colitis: analysis of 49 cases

Journal of Coloproctology, 2012
OBJECTIVE: To evaluate the results of ileal J-pouch anal anastomosis in ulcerative colitis and familial adenomatous polyposis. METHOD: Retrospective analysis of medical records of 49 patients submitted to ileal J-pouch anal anastomosis.
Bruno Amaral Medeiros, Leonardo Estenio Iezzi, Marley Ribeiro Feitosa, Rogério Serafim Parra, Ana Luiza Normanha Ribeiro de Almeida, Raphael Gurgel de Carvalho, Jose Joaquim Ribeiro da Rocha, Omar Feres   +7 more
doaj  

[A young man with intestinal polyposis and epistaxis]

, 2014
Contains fulltext : 137321.pdf (Publisher’s version ) (Closed access)BACKGROUND: Germline mutations in the SMAD4 gene lead to both juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia (HHT). CASE DESCRIPTION: A 23-year-
Mager, J.J., Nicolai, J.J., Jacobs, M.A., Aalfs, C.M., Menko, F.H., Mensenkamp, A.R.   +5 more
core  

Polyposis of Small Intestine [PDF]

BMJ, 1953
openaire   +2 more sources