Glycogen storage disease type III history and symptoms: Difference between revisions
No edit summary |
No edit summary |
||
(One intermediate revision by the same user not shown) | |||
Line 3: | Line 3: | ||
{{CMG}}; {{AE}}{{Anmol}} | {{CMG}}; {{AE}}{{Anmol}} | ||
==Overview== | ==Overview== | ||
The hallmark of glycogen storage disease type 3 is [[hepatomegaly]]. The most common symptoms of glycogen storage disease include [[abdominal]] protuberance and [[muscle weakness]]. | The hallmark of glycogen storage disease type 3 is [[hepatomegaly]]. The most common symptoms of glycogen storage disease include [[abdominal]] protuberance and [[muscle weakness]]. | ||
Line 35: | Line 36: | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category: | |||
[[Category:Endocrinology]] | |||
[[Category:Hepatology]] | |||
[[Category:Gastroenterology]] | |||
[[Category:Pediatrics]] | |||
[[Category:Up-To-Date]] | |||
[[Category:Genetic disorders]] | |||
[[Category:Metabolic disorders]] |
Latest revision as of 15:10, 29 December 2017
Glycogen storage disease type III Microchapters |
Differentiating Glycogen storage disease type III from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type III history and symptoms On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type III history and symptoms |
FDA on Glycogen storage disease type III history and symptoms |
CDC on Glycogen storage disease type III history and symptoms |
Glycogen storage disease type III history and symptoms in the news |
Blogs on Glycogen storage disease type III history and symptoms |
Risk calculators and risk factors for Glycogen storage disease type III history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Overview
The hallmark of glycogen storage disease type 3 is hepatomegaly. The most common symptoms of glycogen storage disease include abdominal protuberance and muscle weakness.
History and Symptoms
- The hallmark of glycogen storage disease type 3 is hepatomegaly. The most common symptoms of glycogen storage disease include abdominal protuberance and muscle weakness.
History
Patients with glycogen storage disease type 3 may have a positive history of:[1][2]
- Seizures or other manifestations of severe fasting hypoglycemia
- Hepatomegaly with abdominal protuberance
- Muscle weakness
Common Symptoms
Common symptoms of glycogen storage disease type 3 include:[1]
- Protruded abdomen due to hepatomegaly
- Muscle weakness
- Hypotonia
- Wasting of skeletal muscle
- Symptoms due to cardiac involvement
Less Common Symptoms
Less common symptoms of glycogen storage disease type 3 include:[1]
- Associated peripheral neuropathy
- Symptoms due to polycystic ovary disease
- Ketoacidosis
- Hyperlipidemia
- Growth retardation
References
- ↑ 1.0 1.1 1.2 Kishnani, Priya S; Austin, Stephanie L; Arn, Pamela; Bali, Deeksha S; Boney, Anne; Case, Laura E; Chung, Wendy K; Desai, Dev M; El-Gharbawy, Areeg; Haller, Ronald; Smit, G Peter A; Smith, Alastair D; Hobson-Webb, Lisa D; Wechsler, Stephanie Burns; Weinstein, David A; Watson, Michael S (2010). "Glycogen Storage Disease Type III diagnosis and management guidelines". Genetics in Medicine. 12 (7): 446–463. doi:10.1097/GIM.0b013e3181e655b6. ISSN 1098-3600.
- ↑ Dagli A, Sentner CP, Weinstein DA. Glycogen Storage Disease Type III. 2010 Mar 9 [Updated 2016 Dec 29]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017. Available from: https://www.ncbi.nlm.nih.gov/books/NBK26372/