Article:
Rett Syndrome: A Case report Authors

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorShrestha, M
dc.contributor.authorRajbhandari, A
dc.date.accessioned2026-06-22T08:03:45Z
dc.date.available2026-06-22T08:03:45Z
dc.date.issued2008
dc.descriptionM Shrestha Teaching Assistant, Department of Paediatrics Trivubhan University Teaching Hospital (TUTH) IOM A Rajbhandari Programme Incharge, Self Help Group for Cerebral Palsy (SGCP)
dc.description.abstractAbstract: Rett syndrome (RS) is a severe neuro-developmental disorder leading to severe intellectual disability in females all around the world. A four-year-old girl from Kathmandu presented with classic features of Rett syndrome (RS), including developmental regression with dementia, loss of acquired speech and hand function, and stereotypic hand movements along with generalized tonic clonic convulsion.
dc.identifier0.3126/jnps.v28i1.1401
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6729
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectRett Syndrome
dc.subjectDevelopmental Regression
dc.titleRett Syndrome: A Case report Authors
dc.typeArticle
dspace.entity.typePublication
local.article.typeOriginal Article
oaire.citation.endPage19
oaire.citation.startPage17
relation.isJournalIssueOfPublication9b28b908-cb0e-4cd3-9fd9-0291eadf3ca0
relation.isJournalIssueOfPublication.latestForDiscovery9b28b908-cb0e-4cd3-9fd9-0291eadf3ca0
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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