Results 11 to 20 of about 10,885 (206)

Case report of a 7-year-old CIPA child with multiple debridement's and amputations.

open access: yesInternational Journal of Endorsing Health Science Research, 2021
Background: Congenital Insensitivity to Pain (CIPA), otherwise known as Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV), is a rarely occurring autosomal recessive disorder encompassed by a group of hereditary and sensory autonomic ...
Syed Ali Haider Zaidi   +7 more
doaj   +1 more source

A Systematic Review of Congenital Insensitivity to Pain, a Rare Disease [PDF]

open access: yesJournal of Personalized Medicine
Andres Reinoso Cobo   +2 more
exaly   +2 more sources

Congenital Insensitivity to Pain with Anhidrosis (CIPA) Syndrome; A Rare Genetic Disorder Case Story

open access: yesCase Reports in Clinical Practice, 2022
Congenital insensitivity to pain with anhidrosis (CIPA) is the subtype four of hereditary sensory and autonomic neuropathy (HASN IV), caused by a defect in the NTRK1 gene and presenting early in life.
Zahra Nafei, Marjan Jafari
doaj   +1 more source

Loss of Prdm12 during development, but not in mature nociceptors, causes defects in pain sensation

open access: yesCell Reports, 2021
Summary: Prdm12 is a key transcription factor in nociceptor neurogenesis. Mutations of Prdm12 cause congenital insensitivity to pain (CIP) from failure of nociceptor development.
Mark A. Landy   +4 more
doaj   +1 more source

A rare case of congenital insensitivity to pain with anhydrosiss

open access: yesIndian Journal of Pain, 2015
Congenital insensitivity to pain syndrome with anhydrosis (CIPA) is a rare inherited disorder. It is characterized by loss of pain and temperature sensation, lack of sweating and mild mental retardation.
Govardhani Yanamadala   +3 more
doaj   +1 more source

Anesthetic management of a patient with congenital insensitivity to pain with anhidrosis by coadministration of remifentanil

open access: yesJA Clinical Reports, 2018
Background Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease characterized by unexplained fever, systemic insensitivity to pain, anhidrosis, and mental distress.
Yoko Takeuchi   +5 more
doaj   +1 more source

Congenital insensitivity to pain with anhidrosis and compensatory hyperhidrosis

open access: yesIndian Journal of Paediatric Dermatology, 2021
Hereditary sensory and autonomic neuropathy is a rare syndrome characterized by congenital insensitivity to pain, temperature changes, and an autonomic nerve formation disorder. We report an 8-year-old boy who presented with late-onset of self-mutilating
Aradhana Rout   +3 more
doaj   +1 more source

Exploring CNS Involvement in Pain Insensitivity in Hereditary Sensory and Autonomic Neuropathy Type 4: Insights from Tc−99m ECD SPECT Imaging

open access: yesTomography, 2023
Hereditary sensory and autonomic neuropathy type 4 (HSAN4), also known as congenital insensitivity to pain with anhidrosis (CIPA), is a rare genetic disorder caused by NTRK1 gene mutations, affecting nerve growth factor signaling. This study investigates
Cheng-Chun Chiang   +5 more
doaj   +1 more source

How Mobile Health Technology Can Help with Health Care of the Congenital Insensitivity to Pain with Anhidrosis (CIPA)? [PDF]

open access: yesTaṣvīr-i salāmat, 2022
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare genetic disease that is inherited as an autosomal recessive, and its cause is a genomic defect in tyrosine kinase; this disorder is mainly characterized by a lack of pain sensation ...
Fatemeh Ameri, Dastani Meisam
doaj   +1 more source

Congenital Insensitivity to Pain (HSNA type IV)

open access: yesPediatric Neurology Briefs, 2015
Investigators from New York University, NY, studied 14 patients with congenital insensitivity to pain with anhidrosis (CIPA), compared to 10 patients with chronically deficient sympathetic activity (pure autonomic failure), and 15 normal age-matched ...
J Gordon Millichap
doaj   +1 more source

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