Rett syndrome in Ireland: a demographic study

Rett syndrome (RTT) is a rare neurodevelopmental condition associated with mutations in the gene coding for the methyl-CpG-binding protein 2 (MECP2). It is primarily observed in girls and affects individuals glob...

Source: Orphanet Journal of Rare Diseases - January 31, 2024 Category: Internal Medicine Authors: Komal Zade, Ciara Campbell, Snow Bach, Hazel Fernandes and Daniela Tropea Tags: Research Source Type: research