Mutational Analysis of TRAPPC9 IN Non-syndromic Intellectual Disability in Selected Patients
DOI:
https://doi.org/10.53762/grjnst.04.03.04Keywords:
Mutation, Syndrome, Neurodevelopment, Patients, Cognitive behaviorAbstract
Intellectual incapacity (identity) is a neurodevelopmental circumstance characterized through good sized obstacles in cognitive functioning and adaptive behavior, with onset before the age of 18. It is usually diagnosed in early formative years due to developmental delays in motor, cognitive, and speech abilities, and is generally described by way of an IQ under 70. Identity is classed into syndromic and non-syndromic kinds and further divided into mild, mild, extreme, and profound categories based totally on severity. This takes a look at centered on non-syndromic identification patients, regarding medical evaluation and genetic evaluation. Blood samples have been accrued, and DNA became analyzed the usage of PCR with TRAPPC9 gene primers, followed by gel electrophoresis and sequencing. No mutation became detected in exon 14 of the TRAPPC9 gene, suggesting the want for broader genetic investigations to higher understand and help reduce the prevalence of intellectual incapacity.
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Copyright (c) 2026 Mubara Mubashar, Farva Razzaq Maham, Saman Mumtaz, Farooq Ahmad, Fizza Hassan, Laraib Saleem, Hafiza Komal Naeem (Author)

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