Zobrazeno 1 - 10
of 100
pro vyhledávání: '"hereditary sensory autonomic neuropathy"'
Publikováno v:
Frontiers in Dental Medicine, Vol 4 (2023)
Hereditary sensory autonomic neuropathy (HSAN) is a group of rare genetic disorders in which affected patients have a diminished capacity to feel pain. Patients with HSAN may present with a wide range of factitial injuries, where injury to the oral c
Externí odkaz:
https://doaj.org/article/ed4dbf765848487194674353a7a5c979
Publikováno v:
Orthopaedic Surgery, Vol 12, Iss 3, Pp 1010-1015 (2020)
Congenital pain insensitivity is a rare genetic disease and its clinical manifestations are many. In orthopaedics, common complications of this disease include painless fracture and Charcot's arthropathy. We followed up a case of multiple fractures o
Externí odkaz:
https://doaj.org/article/ef803749ce44493f97bd9ef74289eb92
Akademický článek
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Autor:
Wanlin Yang, Kijung Sung, Fengli Zhou, Wei Xu, Robert A. Rissman, Jianqing Ding, Chengbiao Wu
Publikováno v:
Frontiers in Aging Neuroscience, Vol 10 (2018)
Nerve growth factor (NGF) exerts multifaceted functions through different stages of life. A missense mutation (R100W) in the beta-NGF gene was found in hereditary sensory autonomic neuropathy V (HSAN V) patients with severe loss of pain perception bu
Externí odkaz:
https://doaj.org/article/adec7960054d455f8f3166af55f92b01
Publikováno v:
Indian Journal of Pain, Vol 28, Iss 1, Pp 13-17 (2014)
Pain causes a reflex withdrawal from any stimuli that can cause actual or potential tissue damage. It is frequently an early symptom of a disease process and is often the impetus for a patient to seek medical treatment. In many disorders where pain a
Externí odkaz:
https://doaj.org/article/af1f86905a084abdbb2884fa3c05e933
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 2, Pp ZL01-ZL02 (2016)
Externí odkaz:
https://doaj.org/article/8fb07eed96aa4d7d886407ef038ded52
Publikováno v:
Orthopaedic Surgery, Vol 12, Iss 3, Pp 1010-1015 (2020)
Orthopaedic Surgery
Orthopaedic Surgery
Congenital pain insensitivity is a rare genetic disease and its clinical manifestations are many. In orthopaedics, common complications of this disease include painless fracture and Charcot's arthropathy. We followed up a case of multiple fractures o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0062310170f1e99f2886c4585b0f79b3
https://doaj.org/article/ef803749ce44493f97bd9ef74289eb92
https://doaj.org/article/ef803749ce44493f97bd9ef74289eb92
Publikováno v:
Indian Journal of Dermatology, Vol 54, Iss 5, Pp 1-4 (2009)
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 n
Externí odkaz:
https://doaj.org/article/a24a4af8273d4750936e424f90dadfd1
Autor:
G P Prashanth, Mahesh Kamate
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 2, Pp 134-136 (2012)
Hereditary sensory autonomic neuropathy type IV (HSAN -IV), also known as congenital insensitivity to pain with anhidrosis, is a very rare condition that presents in infancy with anhidrosis, absence of pain sensation and self -mutilation. Development
Externí odkaz:
https://doaj.org/article/292608770faf4c9c9eac1f1e4781a248