IGSF1deficiency was first described in 2012 and up to date is the most common genetic cause of X-linked isolated central congenital hypothyroidism. The estimated incidence is approximately 1 in 100000.
IGSF1IGSF1IGSF1deficiency was first described in 2012 and up to date is the most common genetic cause of X-linked isolated central congenital hypothyroidism. The estimated incidence is approximately 1 in 100000.