Mitochondrial myopathy: Difference between revisions

(19 intermediate revisions by 4 users not shown)

Line 1:

{{ICD10 transition status

| OldDxArticle =| CurrentStatus = ~~manually added for testing~~

| OldDxArticle =Myopathy

| CurrentStatus = reconciled

| InitialEditorAssigned = Joyce Peterson

~~| MinimumCombinedCodes =~~

}}

{{ICD10 dx

| MinimumCombinedCodes =

| ICD10 Code=G71.3

| BugRequired=

}}

== 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 ==

*[[Paraneoplastic neuropathy or myopathy]]

*[[Myopathy, drug-induced]]

*[[Myopathy, alcoholic]]

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

*[[Metabolic disorder, NOS]]

== ~~Alternate ICD10s to consider coding instead~~ ==

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

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

== Related CCI Codes ==

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

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

== Related Articles ==

@@ Line 1: / Line 1: @@
 {{ICD10 transition status
-| OldDxArticle =| CurrentStatus = manually added for testing
+| OldDxArticle =Myopathy
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Joyce Peterson
-| MinimumCombinedCodes =
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=G71.3
 | BugRequired=
 }}
+{{ICD10 category|Neuro}}
 == 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 ==
+*[[Paraneoplastic neuropathy or myopathy]]
+*[[Myopathy, drug-induced]]
+*[[Myopathy, alcoholic]]
+*[[Muscle disorder/myopathy (primary or secondary), NOS]]
+*[[Metabolic disorder, NOS]]
-== Alternate ICD10s to consider coding instead ==
+== Candidate [[Combined ICD10 codes]] ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+== Related CCI Codes ==
-== Candidate [[Combined ICD10 codes]] ==
+{{Data Integrity Check List}}
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}