Mauriac Syndrome: Rare Complication in Type-1 Diabetic Children
نویسندگان
چکیده
منابع مشابه
Hepatic glycogenosis in type 1 diabetes mellitus mimicking Mauriac syndrome
Hepatic glycogenosis in type 1 diabetes mellitus (DM) can be caused by poor glycemic control due to insulin deficiency, excessive insulin treatment for diabetic ketoacidosis, or excessive glucose administration to control hypoglycemia. Mauriac syndrome, which is characterized by hepatomegaly due to hepatic glycogenosis, growth retardation, delayed puberty, and Cushingoid features, is a rare dia...
متن کاملMauriac syndrome and early cataract diabetic
Result A 5 year and 10 month old boy, was admitted with protuberant abdomen since one year ago. He had been recognized as type 1 DM and treated by subcutaneous insulin 4-5 U/day twice a day until admission. His abdomen became larger, wasted arms and legs so he couldn’t support his body, and just laid down for 3 months. He had retarded growth and development. Oedema face, chest was normal, diste...
متن کاملMauriac syndrome still exists.
BACKGROUND/OBJECTIVE Mauriac syndrome (MS) is a rare complication of type 1 diabetes mellitus (DM1). It is related to low insulin concentrations and is less common since longer-acting insulins became available. It is characterized by hepatomegaly, growth and puberty delay, and the presence of elevated transaminases and serum lipids. The aim of this study was to describe the patients from a pedi...
متن کاملDiscovery of a Genetic Metabolic Cause for Mauriac Syndrome in Type 1 Diabetes.
A mechanistic cause for Mauriac syndrome, a syndrome of growth failure and delayed puberty associated with massive liver enlargement from glycogen deposition in children with poorly controlled type 1 diabetes, is unknown. We discovered a mutation in the catalytic subunit of liver glycogen phosphorylase kinase in a patient with Mauriac syndrome whose liver extended into his pelvis. Glycogen phos...
متن کاملHémothorax spontané: complication rare de la neurofibromatose type 1
Résumé La neurofibromatose de type 1 (NF1) ou maladie de Von Recklinghausen est une maladie héréditaire la plus fréquente des phacomatoses, de transmission autosomique dominante. Ses complications pulmonaires sont rarement décrites dans la littérature. Les complications vasculaires sont retrouvées chez 3,6% des patients. Nous rapportons le cas d'une patiente âgée de 38 ans, suivie pour neurofib...
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ژورنال
عنوان ژورنال: Pediatrics & Therapeutics
سال: 2017
ISSN: 2161-0665
DOI: 10.4172/2161-0665.1000335