Total: 1 |
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PMID (PMCID) | ||
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27899087 (5129599) |
FEMALE | |
Paradoxical physiological responses to propranolol in a Rett syndrome patient: a case report. | ||
Santosh PJ, Bell L, Lievesley K, Singh J, Fiori F. BMC Pediatr. 2016;16(1):194. |
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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. |