Patellofemoral Syndrome Icd 9 Code

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Fragile X syndrome is a genetic condition involving changes in part of the X chromosome. It is the most common form of inherited mental retardation in males and a significant cause of mental retardation in females.

Alternative Names

Martin-Bell syndrome; Marker X syndrome

Causes, incidence, and risk factors

Fragile X syndrome is caused by a change in the FMR1 gene. A small section of the gene code (three letters only -- CGG) is repeated on a fragile...

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