Congenital insensitivity to pain-hypohidrosis syndrome

A hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has material basis in homozygous mutation in the PRDM12 gene on chromosome 9q34.

Also known as: CIP-hypohidrosis syndrome, HSAN8, hereditary sensory and autonomic neuropathy type 8, hereditary sensory and autonomic neuropathy type VIII, HSAN 8, neuropathy, hereditary sensory and autonomic, type 8, neuropathy, hereditary sensory and autonomic, type VIII

7 clinical trials for this condition and its sub-types, 0 tagged with Congenital insensitivity to pain-hypohidrosis syndrome itself.