Publication: The Cri du Chat syndrome in a 6-year-old boy
| creativeworkseries.issn | ISSN (Print) : 1993-2979 | ISSN (Online) : 1993-2987 | |
| dc.contributor.author | Koirala, Naba Raj | |
| dc.contributor.author | Sharma, Vidhya Dev | |
| dc.contributor.author | Khalid, Abdul | |
| dc.contributor.author | Nepal, Mahendra K | |
| dc.contributor.author | Pradhan, Sudarshan N | |
| dc.contributor.author | Pokharel, Anupam | |
| dc.date.accessioned | 2026-07-21T06:22:37Z | |
| dc.date.available | 2026-07-21T06:22:37Z | |
| dc.date.issued | 2000 | |
| dc.description.abstract | Abstract The partial deletion of short arm of chromosome 5, which is known as Cri du Chat syndrome, although rare is a major cause of mental retardation in children. This case report describes the cognitive and behavioural profile of a six-year old boy who displayed evidences of severe mental retardation, behavioural problem and seizure disorder. Keywords: Cri du Chat, deletion, chromosome, epilepsy | |
| dc.identifier | https://doi.org/10.59779/jiomnepal.123 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/6992 | |
| dc.language.iso | en_US | |
| dc.publisher | Institute of Medicine | |
| dc.subject | Cri du Chat | |
| dc.subject | deletion | |
| dc.subject | chromosome | |
| dc.subject | epilepsy | |
| dc.title | The Cri du Chat syndrome in a 6-year-old boy | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
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