Arthropathy-related pain in a patient with congenital impairment of pain sensation due to hereditary sensory and autonomic neuropathy type II with a rare mutation in the WNK1/HSN2 gene: a case report

BACKGROUND: Hereditary sensory and autonomic neuropathy (HSAN) type II with WNK1/HSN2 gene mutation is a rare disease characterized by early-onset demyelination sensory loss and skin ulceration. To the best of our knowledge, no cases of an autonomic disorder have been reported clearly in a patient w...

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Detalles Bibliográficos
Autores principales: Yamada, Keiko, Yuan, Junhui, Mano, Tomoo, Takashima, Hiroshi, Shibata, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073964/
https://www.ncbi.nlm.nih.gov/pubmed/27765018
http://dx.doi.org/10.1186/s12883-016-0727-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073964/
https://www.ncbi.nlm.nih.gov/pubmed/27765018
http://dx.doi.org/10.1186/s12883-016-0727-8

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