Results 11 to 20 of about 7,139 (182)

Intractable diarrhea caused by a rare rectal foreign body [PDF]

Kaohsiung Journal of Medical Sciences
Qi Fan, Shuang Yu, De‐Hai Xiong
doaj   +2 more sources

Unmasking of Asymptomatic Celiac Disease and Microscopic Colitis After Acquiring COVID-19

Annals of Internal Medicine: Clinical Cases, 2023
Previous studies have suggested that viruses may trigger the development of autoimmune diseases such as celiac disease. We report a 75-year-old elderly man who developed intractable diarrhea after acquiring COVID-19.
Tze Shien Lo, Joshua D. LeClaire, Rajib K. Lala, Fadel Nammour, Kristine Saunders   +4 more
doaj   +1 more source

Congenital Sodium Diarrhea: Antenatal Diagnosis May Prevent Unnecessary Surgery in the Neonate

American Journal of Perinatology Reports, 2023
Congenital sodium diarrhea (CSD) is a rare, life-threatening condition characterized by intractable diarrhea, hyponatremia, and metabolic acidosis. It presents similarly to other congenital disorders and, therefore, is often misdiagnosed and mistreated.
Dana S. Berger, Virginia Tancioco, Vineet K. Shrivastava   +2 more
doaj   +1 more source

Enteroendocrine Dysfunction in Two Saudi Sisters

Case Reports in Gastroenterology, 2021
Proprotein convertase (PC) deficiency is a rare autosomal recessive disorder caused by mutations in proprotein convertase subtilisin/kexin type 1 (PCSK1).
Amna Basheer M. Ahmed, Badr M. Rasheed Alsaleem   +1 more
doaj   +1 more source

Successful Treatment of Severe Intractable Diarrhea and Malnutrition in a Child with Dilated Cardiomyopathy Bridged to Left Ventricular Assist Device from Extracorporeal Cardiopulmonary Resuscitation

Journal of Pediatric Emergency and Intensive Care Medicine, 2022
An increasing number of pediatric patients with dilated cardiomyopathy (DCMP) undergo mechanical circulatory support (MCS), as a bridge to heart transplantation. Gastrointestinal complications in this population are rare, and the treatment is challenging.
Edin Botan, Tanıl Kendirli, Emrah Gün, Mehmet Gökhan Ramoğlu, Tayfun Uçar, Mehmet Cahit Sarıcaoğlu, Ceyda Tuna Kırsaçlıoğlu, Zarife Kuloğlu, Erdal İnce, Ahmet Rüçhan Akar   +9 more
doaj   +1 more source

Collagenous colitis following SARS‐Cov2 mRNA vaccination

JGH Open, 2023
A healthy 49‐year‐old female developed intractable watery diarrhea after the Pfizer SARS‐Cov2 mRNA vaccination. She was subsequently diagnosed with collagenous colitis (CC).
Momoko Iketani, Yutaka Takada, Toshinao Itani   +2 more
doaj   +1 more source

Tricho-hepato-enteric syndrome: Retrospective multicenter experience in Saudi Arabia

The Saudi Journal of Gastroenterology, 2022
Background: Trichohepatoenteric syndrome (THES) is a very rare disorder that is characterized by intractable congenital diarrhea, woolly hair, intrauterine growth restriction, facial dysmorphism, and short stature. Our knowledge of THES is limited due to
Badr M Alsaleem, Mohammed Hasosah, Amna Basheer M. Ahmed, Maher M Al Hatlani, Aziz Helal Alanazi, Abdulrahman Al-Hussaini, Ali T Asery, Khalid A Alghamdi, Muhanad M AlRuwaithi, Musa Ali M. Khormi, Ahmed Al Sarkhy, Ali S Alshamrani   +11 more
doaj   +1 more source

A case of autoimmune enteropathy with CTLA4 haploinsufficiency [PDF]

Intestinal Research, 2022
Autoimmune enteropathy (AIE) is a rare disease, characterized by intractable diarrhea, villous atrophy of the small intestine, and the presence of circulating anti-enterocyte autoantibodies. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked
Haruka Miyazaki, Namiko Hoshi, Michitaka Kohashi, Eri Tokunaga, Yuna Ku, Haruka Takenaka, Makoto Ooi, Nobuyuki Yamamoto, Suguru Uemura, Noriyuki Nishimura, Kazumoto Iijima, Keisuke Jimbo, Tsubasa Okano, Akihiro Hoshino, Kohsuke Imai, Hirokazu Kanegane, Ichiro Kobayashi, Yuzo Kodama   +17 more
doaj   +1 more source

Case Report: A Novel Homozygous Frameshift Mutation of the SKIV2L Gene in a Trichohepatoenteric Syndrome Patient Presenting With Short Stature, Premature Ovarian Failure, and Osteoporosis

Frontiers in Genetics, 2022
Background: Trichohepatoenteric syndrome (THES) is a rare Mendelian autosomal recessive genetic disease characterized by intractable diarrhea, woolly hair, facial abnormality, immune dysfunction, and intrauterine growth restriction.
Minyi Yang, Yu Jiang, Xinyu Shao, Xinyu Shao   +3 more
doaj   +1 more source

Case Report: Novel Compound-Heterozygous Variants of SKIV2L Gene that Cause Trichohepatoenteric Syndrome 2

Frontiers in Genetics, 2021
Background: Trichohepatoenteric syndrome (THES) is a rare disease that mainly causes intractable diarrhea. It is classified into THES1 and THES2, which are associated with the tetratricopeptide repeat domain 37 (TTC37) gene and Ski2-like RNA helicase ...
Qiao Zhang, Xia Qian, Jianli Zhou, Lin Han, Shaoming Zhou, Zhaoxia Wang   +5 more
doaj   +1 more source