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

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...

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Dettagli Bibliografici
Pubblicato in:Contemp Clin Dent
Autori principali: Kalaskar, Ritesh, Kalaskar, Ashita
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4319325/
https://ncbi.nlm.nih.gov/pubmed/25684922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.149302
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