A CHILD WITH X LINKED INHERITED INTELLECTUAL DISABILITY

Authors

  • Samadhara V Jogi Subbaiah Institute of Medical Sciences
  • Vikram S Kumar Subbaiah Institute of Medical Sciences
  • Niranjan Kamble Subbaiah Institute of Medical Sciences
  • Darshan Rajatadri Rangaswamy Subbaiah Institute of Medical Sciences

DOI:

https://doi.org/10.54530/jcmc.1485

Keywords:

Autistic disorder; Genetics; Mutation; Neurodevelopmental disorder.

Abstract

X-linked intellectual disability, also known as X-linked mental retardation, is a neurodevelopmental disorder caused by a gene defect on the X chromosome. While more than 100 genes have been linked to X linked intellectual disability, the genetic aetiology of intellectual disability remains unknown in approximately half of the cases. Intellectual disability often co-occurs with other conditions like epilepsy and autism spectrum disorder.

X-linked 98-related intellectual disability syndrome is a rare neurodevelopmental disorder due to Neurite extension and migration factor gene mutation characterised by global developmental delay, intellectual disability, and language delay, with or without autistic features. Distinctive characteristics include coarse facial features, a protruding tongue, and behavioural abnormalities such as excessive tantrums and intrusiveness.

The case study presented involves a child with a stop-gain variant in the Neurite extension and migration factor gene presenting with autism spectrum disorder, specific learning disability and behavioural abnormalities with interesting phenotypic features.

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Published

2024-06-17

How to Cite

1.
A CHILD WITH X LINKED INHERITED INTELLECTUAL DISABILITY. JCMC [Internet]. 2024 Jun. 17 [cited 2024 Sep. 8];14(2):94-5. Available from: https://jcmc.com.np/jcmc/index.php/jcmc/article/view/1485

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