MRXS1 (medical condition): A rare genetic syndrome involving mental retardation, abnormal movements, seizures and ataxia. The syndrome is inherited in a X-linked manner which means that females are carriers but only males display the symptoms.
See also:
Partington X-linked mental retardation syndrome:
»Introduction: Partington X-linked mental retardation syndrome
»Symptoms of Partington X-linked mental retardation syndrome
MRXS1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that MRXS1, or a subtype of MRXS1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
MRXS1: Another name for Partington X-linked mental retardation syndrome (or close medical condition association).
»Introduction: Partington X-linked mental retardation syndrome
»Symptoms of Partington X-linked mental retardation syndrome
Some of the symptoms of MRXS1 incude:
See full list of 9 symptoms of MRXS1 (Partington X-linked mental retardation syndrome)
Source - NIH
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