Indian researchers find rare gene mutation linked to recurrent neurological decline in kids

Indian researchers find rare gene mutation linked to recurrent neurological decline in kids

New Delhi, Nov 27 (IANS) A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers… Continue reading Indian researchers find rare gene mutation linked to recurrent neurological decline in kids The post Indian researchers find rare gene mutation linked to recurrent neurological decline in kids first appeared on Australia India News.

Redcliffe Labs identifies rare USP18 gene mutation linked to neurological decline in children

Redcliffe Labs has reported the discovery of a rare USP18 gene mutation associated with recurrent neurological decline in children. The findings, published in Clinical Dysmorphology, document a previously unreported variant, c.358C>T (p.Pro120Ser), expanding clinical understanding of Pseudo-TORCH syndrome type 2. The condition is often difficult to diagnose due to overlapping symptoms with infectious and metabolic disorders. The clinical evaluat…