Results 31 to 40 of about 3,502,764 (202)
Protein-Losing Enteropathy Resolved by Helicobacter pylori Eradication
European Journal of Case Reports in Internal Medicine, 2022 Protein-losing enteropathy (PLGE) is an uncommon condition with a multifactorial origin, that is characterized by excessive loss of serum proteins into the gastrointestinal tract, resulting in hypoproteinaemia and oedema.
Bruno Sousa +3 more
doaj +1 more source
A Yet Unrecognized Cause of Unusually High Levothyroxine Replacement Dose: Protein-Losing Enteropathy [PDF]
, 2023 Background/objectiveLarge amount of protein wasting such as in nephrotic syndrome is a rare cause of high levothyroxine (LT4) replacement dose requirement. A case has been reported here that demonstrates that protein-losing enteropathy is a novel and yet
Run Yu, Yu, Run
core +1 more source
Animals, 2022 Intestinal lymphangiectasia was first described in the dog over 50 years ago. Despite this, canine IL remains poorly understood and challenging to manage.
Sara A. Jablonski
doaj +1 more source
Intestinal lymphangiectasia in dogs, challenging diagnosis: Four cases [PDF]
Veterinarski Glasnik, 2017 Intestinal lymphangiectasia is an uncommon disease which can cause severe, chronic protein-losing enteropathy in dogs. Four dogs were presented at the Belgrade Clinic for Small Animals with clinical signs of chronic diarrhea, lethargy, anorexia,
Davitkov Darko +5 more
doaj +1 more source
Sarcoidosis and protein losing enteropathy
Gastroenterology, 1980 The authors report a case of sarcoidosis associated with protein losing enteropathy. The diagnosis of intrathoracic stage I sarcoidosis was based on x-ray and biopsy of mediastinal lymph nodes. Enteric protein loss was suspected because of edema lasting for 2 yr, hypoproteinemia, decreased concentrations of serum immunoglobulins, and lymphopenia ...
O S, Popović +6 more
openaire +2 more sources
A Family with Protein-Losing Enteropathy
Gastroenterology, 1974 This a report of a family of two sibships resulting from consanguineous matings of first cousins once removed. Eight of 28 children in the two sibships were affected by edema, growth retardation, diarrhea, abdominal pain, or clubbing, in varying combinations. In 4 patients, ascites developed and all 4 died.
M, Shani +3 more
openaire +2 more sources
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young +6 more
wiley +1 more source
Journal of Lipid Research, 2017 Acyl-CoA:diacylglycerol acyltransferase (DGAT)1 and DGAT2 catalyze triglyceride (TG) biosynthesis in humans. Biallelic loss-of-function mutations in human DGAT1 result in severe congenital diarrhea and protein-losing enteropathy.
Nina L. Gluchowski +10 more
doaj +1 more source
Journal of Indian Association of Pediatric Surgeons, 2021 We report the case of a 4-year-old boy with protein-losing enteropathy, leading to severe malnutrition. Associated thrombotic microangiopathic features made diagnosis difficult and challenging.
Houda Nassih +3 more
doaj +1 more source
Journal of Parenteral and Enteral Nutrition, EarlyView.Abstract Familial hemophagocytic lymphohistiocytosis type 5 is caused by biallelic pathogenic variants in STXBP2, which encodes syntaxin‐binding protein, a key regulator of vesicle trafficking. In addition to immune dysregulation, patients with familial hemophagocytic lymphohistiocytosis type 5 may present with severe, persistent diarrhea associated ...
Hiroyuki Tanaka +5 more
wiley +1 more source