Glycogen storage disease type V: Difference between revisions
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{{Infobox Disease | {{Infobox Disease | ||
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==overview== | |||
'''Glycogen storage disease type V''' is a [[metabolic disorder]], more specifically a [[glycogen storage disease]], caused by a deficiency of [[myophosphorylase]]. | '''Glycogen storage disease type V''' is a [[metabolic disorder]], more specifically a [[glycogen storage disease]], caused by a deficiency of [[myophosphorylase]]. | ||
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People with this disease experience difficulty when their muscles are called upon to perform relatively brief yet intense activity. The inability to break down glycogen into glucose results in an energy shortage within the muscle, resulting in muscle pain and [[cramp]]ing, and sometimes causing serious injury to the muscles. The typical features of McArdle disease include exercise intolerance with [[myalgia]], early fatigue, and stiffness of exercising muscles, which are sometimes relieved by rest. Following a short period of rest, most patients experience a second wind and can resume exercise with less difficulty.The prevailing levels of fatty acids as potential energy sources for muscle may account for the second wind phenomenon. In addition, [[rhabdomyolysis]]—the breakdown of muscle tissue—can cause [[myoglobinuria]], a red-to-brown-colored [[urine]]. The myoglobinuria can cause [[kidney]] damage. The disease is hereditary and is inherited as an [[autosomal recessive]] trait. [[Anaerobic exercise]] must be avoided but regular gentle [[aerobic exercise]] is beneficial. | People with this disease experience difficulty when their muscles are called upon to perform relatively brief yet intense activity. The inability to break down glycogen into glucose results in an energy shortage within the muscle, resulting in muscle pain and [[cramp]]ing, and sometimes causing serious injury to the muscles. The typical features of McArdle disease include exercise intolerance with [[myalgia]], early fatigue, and stiffness of exercising muscles, which are sometimes relieved by rest. Following a short period of rest, most patients experience a second wind and can resume exercise with less difficulty.The prevailing levels of fatty acids as potential energy sources for muscle may account for the second wind phenomenon. In addition, [[rhabdomyolysis]]—the breakdown of muscle tissue—can cause [[myoglobinuria]], a red-to-brown-colored [[urine]]. The myoglobinuria can cause [[kidney]] damage. The disease is hereditary and is inherited as an [[autosomal recessive]] trait. [[Anaerobic exercise]] must be avoided but regular gentle [[aerobic exercise]] is beneficial. | ||
== | ==Historical Perspective== | ||
==Classification== | |||
==Pathophysiology== | |||
==Causes== | |||
==Differentiating {{PAGENAME}} from Other Diseases== | |||
==Epidemiology and Demographics== | |||
==Risk Factors== | |||
==Screening== | |||
==Natural History, Complications, and Prognosis== | |||
==Diagnosis== | |||
===Diagnostic Criteria=== | |||
===History and Symptoms=== | |||
===Physical Examination=== | |||
===Laboratory Findings=== | |||
===Imaging Findings=== | |||
===Other Diagnostic Studies=== | |||
==Treatment== | |||
===Medical Therapy=== | |||
===Surgery=== | |||
===Prevention=== | |||
==External links== | ==External links== | ||
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==References== | |||
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{{Endocrine, nutritional and metabolic pathology|state=collapsed}} | {{Endocrine, nutritional and metabolic pathology|state=collapsed}} | ||
[[Category:Endocrinology]] | |||
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Revision as of 17:30, 21 July 2016
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Glycogen storage disease type V | |
ICD-10 | E74.0 |
---|---|
ICD-9 | 271.0 |
OMIM | 232600 |
DiseasesDB | 5307 |
eMedicine | med/911 |
MeSH | D006012 |
overview
Glycogen storage disease type V is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of myophosphorylase.
GSD type V is also known as McArdle's disease or muscle phosphorylase deficiency. The disease was first reported in 1951 by Dr. Brian McArdle of Guy's Hospital, London.[1]
People with this disease experience difficulty when their muscles are called upon to perform relatively brief yet intense activity. The inability to break down glycogen into glucose results in an energy shortage within the muscle, resulting in muscle pain and cramping, and sometimes causing serious injury to the muscles. The typical features of McArdle disease include exercise intolerance with myalgia, early fatigue, and stiffness of exercising muscles, which are sometimes relieved by rest. Following a short period of rest, most patients experience a second wind and can resume exercise with less difficulty.The prevailing levels of fatty acids as potential energy sources for muscle may account for the second wind phenomenon. In addition, rhabdomyolysis—the breakdown of muscle tissue—can cause myoglobinuria, a red-to-brown-colored urine. The myoglobinuria can cause kidney damage. The disease is hereditary and is inherited as an autosomal recessive trait. Anaerobic exercise must be avoided but regular gentle aerobic exercise is beneficial.
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Glycogen storage disease type V from Other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications, and Prognosis
Diagnosis
Diagnostic Criteria
History and Symptoms
Physical Examination
Laboratory Findings
Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Prevention
External links
References
Template:Endocrine, nutritional and metabolic pathology