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 ORIGINAL ARTICLE
Year : 2021  |  Volume : 69  |  Issue : 6  |  Page : 1729--1736

Assessing Utility of Clinical Exome Sequencing in Diagnosis of Rare Idiopathic Neurodevelopmental Disorders in Indian Population


1 RIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, Gujarat, India
2 Strand Life Sciences Private Limited, Bengaluru, Karnataka, India
3 Mayflower Woman's Hospital, Ahmedabad, Gujarat, India
4 Sheth V. S. General Hospital and NHL Municipal Medical College, Ahmedabad, Gujarat, India
5 Sir Takhtasinhji General Hospital, Bhavnagar, Gujarat, India

Correspondence Address:
Dr. Harsh Sheth
FRIGE's Institute of Human Genetics, FRIGE House, Satellite, Ahmedabad - 380 015. Gujarat
India
Jayesh Sheth
FRIGE's Institute of Human Genetics, FRIGE House, Satellite, Ahmedabad - 380 015. Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0028-3886.333475

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Background: Neurological diseases are phenotypically and genotypically heterogeneous. Clinical exome sequencing (CES) has been shown to provide a high diagnostic yield for these disorders in the European population but remains to be demonstrated for the Indian population. Objective: The study aimed to understand the utility of clinical exome sequencing for the diagnosis of neurodevelopmental disorders. Materials and Methods: A cohort of 19 idiopathic patients with neurological phenotypes, primarily intellectual disability and developmental delay, were recruited. CES covering 4620 genes was performed on all patients. Candidate variants were validated by Sanger sequencing. Results: CES in 19 patients provided identified 21 variants across 16 genes which have been associated with different neurological disorders. Fifteen variants were reported previously and 6 variants were novel to our study. Eleven patients were diagnosed with autosomal dominant de novo variants, 7 with autosomal recessive and 1 with X-linked recessive variants. CES provided definitive diagnosis to 10 patients; hence, the diagnostic yield was 53%. Conclusion: Our study suggests that the diagnostic yield of CES in the Indian population is comparable to that reported in the European population. CES together with deep phenotyping could be a cost-effective way of diagnosing rare neurological disorders in the Indian population.






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