Sisters with no pain, no tears: A report of a new variant of hereditary sensory and autonomic neuropathy (Type IX) Caused by a novel SCN11A mutation

• Asıl Yazarlar: Shital Poojary (Yazar), Saurabh Jaiswal (Yazar), Kapisha Sunny Shah (Yazar), Krishna B Bhalala (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Wolters Kluwer Medknow Publications, 2020-01-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Lack of pain sensation in children involves a rare group of heritable disorders; hereditary sensory and autonomic neuropathy (HSAN). Till date, eight types of HSAN have been described depending on the clinical phenotype and the underlying gene mutation. We report a new variant of HSAN (Type IX) in t...