Rett Syndrome (RS) is a neurological disorder seen almost exclusively in females and found in a variety of racial and ethnic backgrounds. The cause of Rett Syndrome has been traced to a defective gene on the X chromosome called "MeCP2". New Research: Reversal of Neurological Defects in a Mouse Model of Rett Syndrome To read the full paper, click here
			The International Rett Syndrome Association offers comprehensive information and the latest news in RS research. The Rett Syndrome Research Foundation is the world's leading private funder of research for RS.