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SCKL1 (medical condition): Seckel syndrome is a rare inherited disorder mainly involving retarded growth,...more »
SCKL1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SCKL1, or a subtype of SCKL1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SCKL1: SCKL1 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SCKL1 incude:
Source - NIH
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