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What is Mental retardation, X-linked, syndromic 11?

What is Mental retardation, X-linked, syndromic 11?

  • Mental retardation, X-linked, syndromic 11: A rare form of mental retardation inherited in a X-linked manner. It is also associated with an unusual facial appearance and results from a defect on chromosome Xq26-q27. Female carriers tended to have some degree of facial dysmorphism but no mental retardation.

Mental retardation, X-linked, syndromic 11 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Mental retardation, X-linked, syndromic 11, or a subtype of Mental retardation, X-linked, syndromic 11, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Mental retardation, X-linked, syndromic 11: Introduction

What are the symptoms of Mental retardation, X-linked, syndromic 11?

Symptoms of Mental retardation, X-linked, syndromic 11: see symptoms of Mental retardation, X-linked, syndromic 11

Mental retardation, X-linked, syndromic 11: Testing

Diagnostic testing: see tests for Mental retardation, X-linked, syndromic 11.

Misdiagnosis: see misdiagnosis and Mental retardation, X-linked, syndromic 11.

How is it treated?

Treatments for Mental retardation, X-linked, syndromic 11: see treatments for Mental retardation, X-linked, syndromic 11

Name and Aliases of Mental retardation, X-linked, syndromic 11

Main name of condition: Mental retardation, X-linked, syndromic 11

Other names or spellings for Mental retardation, X-linked, syndromic 11:

MRXS11, Shashi X-linked mental retardation syndrome, mental retardation, X-linked, Shashi type

SMRXS, Shashi X linked mental retardation syndrome, X-linked mental retardation syndrome with characteristic facial dysmorphic features, Orofaciodigital syndrome, Shashi type, MRXS11, Mental retardation X linked Shashi type
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)


 » Next page: Prevalence and Incidence of Mental retardation, X-linked, syndromic 11

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