Newly identified genes in Rett-like patients
November 22 2015
Rett and Rett-like disorders Breda Genetics panel recommended for this conditions: Rett and Rett-like syndrome disorders (MECP2, FOXG1, CDKL5, MEF2C, TCF4, GABRD, WDR45, SMC1A) Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting the central nervous system. Being most frequently transmitted as an X-linked dominant disorder caused by MECP2 mutations (90% of cases), RTT primarily affects
