Mitochondrial myopathy: Difference between revisions

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{{ICD10 transition status

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| OldDxArticle =Myopathy

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| InitialEditorAssigned = Joyce Peterson

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== Additional Info ==

~~incl~~ MELAS

'''Includes'''

* MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes)

**Mitochondrial myopathies are a group of neuromuscular diseases caused by damage to the mitochondria—small, energy-producing structures that serve as the cells' "power plants." Nerve cells in the brain and muscles require a great deal of energy, and thus appear to be particularly damaged when mitochondrial dysfunction occurs. Some of the more common mitochondrial myopathies include Kearns-Sayre syndrome, myoclonus epilepsy with ragged-red fibers, and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(MELAS). The symptoms of mitochondrial myopathies include muscle weakness or exercise intolerance, heart failure or rhythm disturbances, dementia, movement disorders, stroke-like episodes, deafness, blindness, droopy eyelids, limited mobility of the eyes, vomiting, and seizures.

== Alternate ICD10s to consider coding instead or in addition ==

(~~turn these into links to the actual diagnosis articles if possible. For some that might make no sense.~~)

*[[Paraneoplastic neuropathy or myopathy]]

*[[Myopathy, drug-induced]]

*[[Myopathy, alcoholic]]

*[[Muscle disorder/myopathy (primary or secondary), NOS]]

*[[Metabolic disorder, NOS]]

== Candidate [[Combined ICD10 codes]] ==

~~(put links to likely candidates coded with this one, eg. a cause for a trauma.)~~

== Related CCI Codes ==

== Related Articles ==

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 {{ICD10 transition status
-| OldDxArticle =
+| OldDxArticle =Myopathy
-| CurrentStatus = freshly automatically generated article
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Joyce Peterson
 }}
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 == Additional Info ==
-incl MELAS
+'''Includes'''
+* MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes)
+**Mitochondrial myopathies are a group of neuromuscular diseases caused by damage to the mitochondria—small, energy-producing structures that serve as the cells' "power plants." Nerve cells in the brain and muscles require a great deal of energy, and thus appear to be particularly damaged when mitochondrial dysfunction occurs. Some of the more common mitochondrial myopathies include Kearns-Sayre syndrome, myoclonus epilepsy with ragged-red fibers, and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(MELAS). The symptoms of mitochondrial myopathies include muscle weakness or exercise intolerance, heart failure or rhythm disturbances, dementia, movement disorders, stroke-like episodes, deafness, blindness, droopy eyelids, limited mobility of the eyes, vomiting, and seizures.
 == Alternate ICD10s to consider coding instead or in addition ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+*[[Paraneoplastic neuropathy or myopathy]]
+*[[Myopathy, drug-induced]]
+*[[Myopathy, alcoholic]]
+*[[Muscle disorder/myopathy (primary or secondary), NOS]]
+*[[Metabolic disorder, NOS]]
 == Candidate [[Combined ICD10 codes]] ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
 == Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
 {{ICD10 footer}}
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