Early onset hereditary sensory autonomic neuropathy type I and not leprosy
Hereditary sensory autonomic neuropathies (HSAN) are rare forms of chronic neuropathies in children, which lead to severe complications like foot ulcers, mutilations, fractures and deformities. We report an eight years old female who presented with nonhealing perforating ulcer over anterior sole, re...
Main Authors: | Pande Sushil, Kharkar Vidya, Mahajan Sunanda, Khopkar Uday |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2009-01-01
|
Series: | Indian Journal of Dermatology |
Subjects: | |
Online Access: | http://www.e-ijd.org/article.asp?issn=0019-5154;year=2009;volume=54;issue=5;spage=1;epage=4;aulast=Pande |
Similar Items
-
Painless ulcers and fissures of toes: Hereditary sensory neuropathy, not leprosy
by: Angoori Gnaneshwar Rao
Published: (2016-01-01) -
Hereditary sensory autonomic neuropathy and anaesthesia - a case report
by: Nandini Dave, et al.
Published: (2007-01-01) -
A case of hereditary sensory autonomic neuropathy type IV
by: G P Prashanth, et al.
Published: (2012-01-01) -
A rare case of hereditary sensory and autonomic neuropathy type II
by: Elmira Mamytova, et al.
Published: (2023-03-01) -
The diagnosis of leprosy among patients with symptoms of peripheral neuropathy without cutaneous lesions: a follow-up study
by: MICHAEL SKACEL, et al.
Published: (2000-09-01)