Results 1 to 10 of about 8,099 (218)

Congenital insensitivity to pain with anhydrosis: report of a family case [PDF]

open access: yesThe Pan African Medical Journal, 2011
Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classified as hereditary sensory and autonomic neuropathy type IV.
Smael Labib   +4 more
doaj   +4 more sources

Congenital Insensitivity to Pain and Anhidrosis [PDF]

open access: yesArchives of Plastic Surgery, 2016
Hereditary sensory and autonomic neuropathy (HSAN) or hereditary sensory neuropathy has five different clinical subtypes. Congenital insensitivity to pain and anhidrosis (CIPA) is HSAN type IV. CIPA is a rare disease with an autosomal recessive inheritance. Recurrent episodes of fever, no sweating, insensitivity to pain, and self-injury are symptoms of
Jin Yong Shin   +4 more
doaj   +3 more sources

Congenital Insensitivity to Pain With Anhidrosis: First Reported Case in Nepal [PDF]

open access: yesClinical Case Reports
Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder characterized by anhidrosis, self‐mutilation, and insensitivity to pain and temperature.
Sobin Pant   +4 more
doaj   +2 more sources

Uncovering oral and maxillofacial clues in congenital insensitivity to pain with anhidrosis: what can sibling cases teach us? [PDF]

open access: yesBMC Oral Health
Background Congenital Insensitivity to Pain with Anhidrosis (CIPA) is an extremely rare congenital disorder characterized by severe clinical and oral manifestations.
Katibe Tugce Temur
doaj   +2 more sources

Anesthetic management of a child with congenital insensitivity to pain with anhidrosis: A case report [PDF]

open access: yesFrontiers in Surgery, 2022
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare, autosomal recessive disease classified as hereditary sensory and autonomic neuropathy type VI. Patients with CIPA are characterized by insensitivity to pain, episodes of unexplained fever,
Ying Zhang, Zhiyu Geng
doaj   +2 more sources

A novel treatment strategy with hyperbaric oxygen of chronic osteomyelitis and pseudoarthrosis in a child with congenital hereditary sensory and autonomic neuropathy type 4 congenital insensitivity to pain with anhidrosis syndrome: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Congenital insensitivity to pain with anhidrosis is a rare but devastating hereditary disease. Congenital insensitivity to pain with anhidrosis is caused by a mutation in the neurotrophic receptor tyrosine kinase 1 gene (NRTK1).
Anders Kjellberg   +3 more
doaj   +2 more sources

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   +4 more sources

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

Successful Management of a Complicated Forearm Fracture in a Patient with Congenital Insensitivity to Pain: A Case Report [PDF]

open access: yesInternational Medical Case Reports Journal
Anas Alrusan,1 Suhaib Bani Essa,2 Saif Aldin Naif Rawabdeh,3 Yazan Anaqreh,2 Modather Hatamleh,1 Mohammad Alradaideh,1 Mohammed Baker,4 Abdelwahab Aleshawi4 1Department of Anesthesiology, Faculty of Medicine, Jordan University of Science and Technology ...
Alrusan A   +7 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

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