Results 31 to 40 of about 5,298 (208)

Congenital Insensitivity to Pain With Anhidrosis Is Associated With Harlequin Color Change: A Survey Study. [PDF]

open access: yesPediatr Dermatol
ABSTRACT Congenital insensitivity to pain with anhidrosis (CIPA), also known as hereditary sensory and autonomic neuropathy (HSAN) type IV, is an extremely rare autosomal recessive congenital condition characterized by the loss of sensation to pain and absence of sweating with one case report linking this with harlequin color change.
Maazi M, Lam JM.
europepmc   +2 more sources

Cholinergic striatal neurons are increased in HSAN V homozygous mice despite reduced NGF bioavailability

open access: goldBiochemical and Biophysical Research Communications - BBRC, 2019
Giovanna Testa   +3 more
openalex   +3 more sources

Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy

open access: yesFrontiers in Neurology, 2022
Non-coding repeat expansions within RFC1 and NOTCH2NLC genes have lately been linked to multisystem neurodegenerative diseases, which also shed light on yet undiagnosed patients with inherited peripheral neuropathies.
Jun-Hui Yuan   +12 more
doaj   +1 more source

Pregnancy in hereditary sensory and autonomic neuropathy type V: A case report and literature review

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2022
Objective: Hereditary sensory and autonomic neuropathies (HSANs) are a clinical heterogenous group of inherited neuropathies featuring prominent sensory and autonomic involvement. We report on the management of pregnancy and delivery in a woman with HSAN
Daisuke Higeta   +5 more
doaj   +1 more source

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

open access: yesIndian Journal of Dermatology, 2020
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 ...
Shital Poojary   +3 more
doaj   +1 more source

Novel Compound Heterozygous DST Variants Causing Hereditary Sensory and Autonomic Neuropathies VI in Twins of a Chinese Family

open access: yesFrontiers in Genetics, 2020
Background: Hereditary sensory and autonomic neuropathies (HSANs) are a rare and severe group of sensory axonal neuropathies. HSANs have been classified into eight groups based on mode of inheritance, clinical features, and the involved genes.
Jie-Yuan Jin   +11 more
doaj   +1 more source

Classifying the Severity of Cyberbullying Incidents by Using a Hierarchical Squashing-Attention Network

open access: yesApplied Sciences, 2022
Cyberbullying has become more prevalent in online social media platforms. Natural language processing and machine learning techniques have been employed to develop automatic cyberbullying detection models, which are only designed for binary ...
Jheng-Long Wu, Chiao-Yu Tang
doaj   +1 more source

The child who felt no pain: A case of hereditary sensory autonomic neuropathy (HSAN) type IV

open access: diamond, 2014
Hereditary sensory autonomic neuropathy (HSAN) is the term used to describe a group of inherited disorders that are associated with sensory dysfunction (reduced reflexes, altered pain and temperature perception) and varying degrees of autonomic ...
Imran Majid, Atiya Yaseen
openalex   +2 more sources

Hereditary sensory and autonomic neuropathies: types II, III, and IV

open access: yesOrphanet Journal of Rare Diseases, 2007
The hereditary sensory and autonomic neuropathies (HSAN) encompass a number of inherited disorders that are associated with sensory dysfunction (depressed reflexes, altered pain and temperature perception) and varying degrees of autonomic dysfunction ...
Axelrod Felicia B   +1 more
doaj   +1 more source

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