Results 11 to 20 of about 8,700 (250)

Congenital Insensitivity to Pain

open access: yesOnline Journal of Health & Allied Sciences, 2011
Congenital Insensitivity to Pain belongs to the family of Hereditary Sensory and Autonomic Neuropathies (HSAN). It is a rare disorder of unknown etiology associated with loss of pain sensation.
Praveen Kumar B,   +2 more
doaj   +1 more source

Congenital insensitivity to pain: Case report of a rare entity

open access: diamondIndian Journal of Paediatric Dermatology, 2018
Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by insensitivity to noxious stimuli and autonomic dysfunction, associated with pathological abnormalities of the peripheral nerves.
Swati Dahiya   +2 more
doaj   +2 more sources

Atypical Presentation of Congenital Insensitivity to Pain With Anhidrosis Leading to Diagnostic Odyssey [PDF]

open access: yesMolecular Genetics & Genomic Medicine
Background Congenital insensitivity to pain with anhidrosis (CIPA) (OMIM 256800) is a rare autosomal‐recessive condition, also known as hereditary sensory and autonomic neuropathy type IV (HSAN‐IV). The most commonly reported features include anhidrosis,
Tomoyasu Higashimoto   +4 more
doaj   +2 more sources

Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes. [PDF]

open access: hybridAm J Med Genet A, 2022
Elsana B   +7 more
europepmc   +2 more sources

Congenital insensitivity to pain with anhidrosis

open access: yesJournal of the Pakistan Medical Association
Congenital Insensitivity to Pain with Anhidrosis (CIPA) is characterised by disruption of sensory neurons caused by genetic mutations in the Neurotrophic Tyrosine Kinase 1 (NTRK1) gene which leads to impaired pain sensation, accompanied by anhidrosis ...
Meher Ayyazuddin   +4 more
doaj   +2 more sources

CONGENITAL INSENSITIVITY TO PAIN WITH ANHYDROSIS

open access: yesGomal Journal of Medical Sciences, 2016
Congenital insensitivity to pain with anhydrosis (CIPA) is a rare genetic disorder characterized by inability to feel pain and temperature, and decreased or absent sweating.
Muhammad shafiq Khan   +2 more
doaj   +1 more source

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