Results 41 to 50 of about 615,949 (181)

Hepatomegaly and abnormal liver tests due to glycogenosis in adults with diabetes [PDF]

, 2019
In adults with diabetes mellitus, hepatomegaly and abnormalities of liver enzymes occur as a consequence of hepatocellular glycogen accumulation, as has been well described in children.
Chatila, Rajaa, West, Brian A.
core   +1 more source

Mauriac Syndrome: Case Report and Review of the Literature

Endocrinology Research and Practice, 2017
This is a case report of a young male with poorly controlled type 1 diabetes mellitus who presented with the clinical features of diabetic ketoacidosis. Once the patient was stabilized, he was examined for hepatomegaly and elevated liver enzymes.
Ömercan TOPALOĞLU, Sibel DEMİRAL SEZER, Bilgin DEMİR, Derya AKARKEN   +3 more
doaj   +1 more source

Electron microscopic study of a case of cerebral glycogenosis [PDF]

, 1966
This case of glycogenosis seams different from all the previously described forms of this disease. There are neither hepatic nor muscular evident glycogen accumulation.
Dourov, Nicolas, Grégoire, Anne
core   +1 more source

Asymptomatic hepatocellular adenoma in Von Gierke glycogenosis type IA in children: clinical-morphological diagnostic particulars. Case report [PDF]

, 2022
Background: The glycogen storage disease and hepatic adenoma, among the liver origin pathologies in the pediatrics, represent a special interest in terms of clinical and pathomorphological diagnosis.
David, V., Petrovici, Vergil, Covali, Loridana, Sinițîna, Lilia, Tatiana, Globa, Gîncu, Gheorghe   +5 more
core  

Prevalence of hepatopathy in type 1 diabetic children

BMC Pediatrics, 2012
Background The Prevalence of liver disease among diabetics has been estimated to be between 17% and 100%. Most of these data were obtained from adult studies. The aim of our study was to screen for liver disease among type 1 diabetic children.
Al-Hussaini Abdulrahman A, Sulaiman Nimer M, AlZahrani Musa D, Alenizi Ahmed S, Khan Mannan   +4 more
doaj   +1 more source

Glucose-6-phosphatase deficiency

Orphanet Journal of Rare Diseases, 2011
Glucose-6-phosphatase deficiency (G6P deficiency), or glycogen storage disease type I (GSDI), is a group of inherited metabolic diseases, including types Ia and Ib, characterized by poor tolerance to fasting, growth retardation and hepatomegaly resulting
Labrune Philippe, Gajdos Vincent, Eberschweiler Pascale, Hubert-Buron Aurélie, Petit François, Vianey-Saban Christine, Boudjemline Alix, Piraud Monique, Froissart Roseline   +8 more
doaj   +1 more source

HEPATIC GLYCOGENOSIS ASSOCIATED WITH TYPE 1 DIABETES (A CASE REPORT)

International Journal of Advanced Research
Background:insulin deficiency in diabetes leads to many complications. Hepatocyte glycogen overload, previously known as Mauriac syndrome, is one of them.
Doctor Samira Handa, Doctor Mohammed Amine Essafi, Doctor Khawla Salhi, Professor Hayat Aynaou, Professor Houda Salhi   +4 more
semanticscholar   +1 more source

Effect of liver transplantation on hepatic glucose metabolism in a patient with type I glycogen storage disease [PDF]

, 2000
BACKGROUND: In type I glycogenosis, mutation of the glucose-6-phosphatase gene results in absent glucose-6-phosphatase activity in liver cells leading to fasting hypoglycemia. Liver transplantation is expected to normalize glucose homeostasis.
Gillet, M., Mosimann, F., Koestinger, A., Tappy, L., Chiolero, R.   +4 more
core   +1 more source

Analysis of GBE1 mutations via protein expression studies in glycogen storage disease type IV: A report on a non-progressive form with a literature review

Molecular Genetics and Metabolism Reports, 2018
Background: Glycogen storage disease type IV (GSD IV), caused by GBE1 mutations, has a quite wide phenotypic variation. While the classic hepatic form and the perinatal/neonatal neuromuscular forms result in early mortality, milder manifestations include
Hiroyuki Iijima, Reiko Iwano, Yukichi Tanaka, Koji Muroya, Tokiko Fukuda, Hideo Sugie, Kenji Kurosawa, Masanori Adachi   +7 more
doaj   +1 more source

Fatty Liver Caused by Glycogen Storage Disease Type IX: A Small Series of Cases in Children

GE: Portuguese Journal of Gastroenterology, 2019
Background: The prevalence of non-alcoholic fatty liver disease (NAFLD) affecting children and adolescents has increased dramatically in recent years.
Catarina Leuzinger Dias, Inês Maio, José Ricardo Brandão, Edite Tomás, Esmeralda Martins, Ermelinda Santos Silva   +5 more
doaj   +1 more source