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LQT7 (medical condition): A rare disorder where a genetic mutation causes periods of muscle weakness,...more »
LQT7 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that LQT7, or a subtype of LQT7,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
LQT7: LQT7 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of LQT7 incude:
These medical disease topics may be related to LQT7:
Source - NIH
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