Paradoxical physiological responses to propranolol in a Rett syndrome patient: a case report

Abstract

BACKGROUND Rett Syndrome (RTT), caused by a loss-of-function in the epigenetic modulator: X-linked methyl-CpG binding protein 2 (MeCP2), is a pervasive neurological disorder characterized by compromised brain functions, anxiety, severe mental retardation, language and learning disabilities, repetitive stereotyped hand movements and developmental regression… (More)

Topics

1 Figure or Table

Slides referencing similar topics