Hereditary sensory and autonomic neuropathy type V: Report of a rare case

• Huvudupphovsmän: Ritesh Kalaskar (Författare, medförfattare), Ashita Kalaskar (Författare, medförfattare)
• Materialtyp: Bok
• Publicerad: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• Ämnen: article
• Länkar: Connect to this object online.

Hereditary sensory and autonomic neuropathy (HSAN) type V is a rare inherited disease caused by a mutation in the neurotrophic tyrosine kinase receptor, type 1 gene located on chromosome 1 (1q21-q22). It is characterized by pain insensitivity, partial anhydrosis without mental retardation and unimpa...