Results 91 to 100 of about 29,765 (217)

A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis

The Turkish Journal of Pediatrics, 2003
Infantile systemic hyalinosis is a rare, progressive, fatal condition with a presumably autosomal recessive mode of inheritance. It is characterized by widespread deposition of hyaline material in many tissues.
Benal Büyükgebiz, Yesim Oztürk, Nur Arslan, Erdener Ozer   +3 more
doaj  

Protein Losing Enteropathy After Fontan Operation: Glimpses of Clarity Through the Lifting Fog

World journal for pediatric & congenital heart surgery, 2019
Fontan-associated protein losing enteropathy is a challenge to treat and is a major contributor to morbidity and mortality in patients with palliated single ventricle.
J. Rychik, K. Dodds, D. Goldberg, Andrew C. Glatz, M. Fogel, J. Rossano, Jonathan M. Chen, E. Pinto, C. Ravishankar, E. Rand, J. Rome, Y. Dori   +11 more
semanticscholar   +1 more source

Atypical hemolytic uremic syndrome in a patient with protein-losing enteropathy

Journal of International Medical Research, 2019
Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease induced by many triggers, all of which produce a common end phenotype of microangiopathic hemolysis and thrombotic microangiopathy.
Ramy M. Hanna, Huma Hasnain, Lama Abdelnour, Beshoy Yanny, Richard M. Burwick   +4 more
doaj   +1 more source

The Clinical Efficacy of Dietary Fat Restriction in Treatment of Dogs with Intestinal Lymphangiectasia

Journal of Veterinary Internal Medicine, 2014
Background Intestinal lymphangiectasia (IL), a type of protein‐losing enteropathy (PLE), is a dilatation of lymphatic vessels within the gastrointestinal tract.
H. Okanishi, R. Yoshioka, Y. Kagawa, T. Watari   +3 more
doaj   +1 more source

Use of octreotide for the treatment of protein‐losing enteropathy in dogs: Retrospective study of 18 cases

Journal of Veterinary Internal Medicine
Background More than 50% of dogs with protein‐losing enteropathy (PLE) fail to respond to standard therapies. Octreotide, a somatostatin analogue, is used in cases of intestinal lymphangiectasia (IL) in humans with some success.
Sara A. Jablonski, Allison S. W. Mazepa, M. Katherine Tolbert   +2 more
doaj   +1 more source

Disseminated Langerhans' cell histiocytosis and massive protein-losing enteropathy

Brazilian Journal of Medical and Biological Research, 1999
Symptomatic involvement of the gastrointestinal (GI) tract as a prominent symptom in Langerhans' cell histiocytosis (LCH) is uncommon, occurring in less than 1 to 5% of all cases, even when the disease is in its disseminated form.
Santos-Machado T.M., Cristófani L.M., Almeida M.T.A., Maluf P.T., Costa P.A., Pereira M.A., Brito J.L.B.C., Odone-Filho V.   +7 more
doaj  

Eosinophilic gastroenteritis presenting as protein--losing enteropathy (case report)

The Turkish Journal of Pediatrics, 1995
Eosinophilic gastroenteropathy is an uncommon, idiopathic disease in children that is characterized by eosinophilic inflammation of the intestine. Predominant involvement of the mucosa is associated with diarrhea and less commonly gastrointestinal
S Karademir, A Akçayöz, K Bek, F C Tanyel, M Sungur, I Celik, C Ural   +6 more
doaj  

Abdominal Lymphatic Malformations Presenting as Protein-Losing Enteropathy. [PDF]

ACG Case Rep J
Thomas J, Roma K, Bhat I.
europepmc   +1 more source

Ovarian T-cell lymphoma in a dog with chronic protein-losing enteropathy. [PDF]

Acta Vet Scand
Mortensen JK, Wikström E, van de Velde N.   +2 more
europepmc   +1 more source

Fontan associated protein-losing enteropathy is linked to distinct metabolic and hepatic alterations. [PDF]

Sci Rep
Schroeder C, Fahlbusch FB, Cesnjevar R, Rauh M, Dittrich S, Moosmann J.   +5 more
europepmc   +1 more source