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Epilepsy progressive myoclonic 2 (medical condition): A rare genetic disorder caused by the inclusion of...more »
See also:
Lafora disease:
»Introduction: Lafora disease
»Symptoms of Lafora disease
These medical condition or symptom topics may be relevant to medical information for Epilepsy progressive myoclonic 2:
Epilepsy progressive myoclonic 2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Epilepsy progressive myoclonic 2, or a subtype of Epilepsy progressive myoclonic 2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Epilepsy progressive myoclonic 2: Another name for Lafora disease (or close medical condition association).
»Introduction: Lafora disease
»Symptoms of Lafora disease
Epilepsy progressive myoclonic 2: Epilepsy progressive myoclonic 2 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Epilepsy progressive myoclonic 2 incude:
See full list of 7 symptoms of Epilepsy progressive myoclonic 2 (Lafora disease)
These medical disease topics may be related to Epilepsy progressive myoclonic 2:
Source - NIH
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