Heterozygous mutations in the X-linked MECP2 gene cause Rett syndrome, a severe neurodevelopmental disorder of young females. Only one male presenting an MECP2 mutation has been reported; he survived only to age 1 year, suggesting that mutations in MECP2 are male lethal. Here we report a three-generation family in which two affected males showed severe mental retardation and progressive spasticity, previously mapped in Xq27.2-qter. Two obligate carrier females showed either normal or borderline intelligence, simulating an X-linked recessive trait. The two males and the two obligate carrier females presented a mutation in the MECP2 gene, demonstrating that, in males, MECP2 can be responsible for severe mental retardation associated with neurological disorders.
|Titolo:||A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males|
|Autori interni:||RIZZOLIO, Flavio|
|Data di pubblicazione:||2000|
|Rivista:||AMERICAN JOURNAL OF HUMAN GENETICS|
|Appare nelle tipologie:||2.1 Articolo su rivista |