Background: Congenital hyposensitivity to pain or hereditary sensory and autonomic neuropathy represents a variety of disorders characterized by decreased perception of …
Y Zhang, N Haga - Journal of Orthopaedic Science, 2014 - Springer
Background Congenital insensitivity to pain with anhidrosis (CIPA) is a rare disorder with various skeletal complications; thus, a compilation of data on affected patients could provide …
A Zlotnik, D Natanel, R Kutz, M Boyko… - Anesthesia & …, 2015 - journals.lww.com
BACKGROUND: Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder characterized by recurrent episodic fevers, anhidrosis, absent reaction to …
T Mimura, S Amano, S Fukuoka, N Honda… - Current eye …, 2008 - Taylor & Francis
Purpose: To observe the morphology of the corneal cells and corneal nerve fibers in patients with type IV or V hereditary sensory and autonomic neuropathy (HSAN) by in vivo confocal …
B Kayani, MD Sewell, J Platinum, A Olivier… - European Journal of …, 2017 - Elsevier
Background Congenital indifference to pain with anhidrosis (CIPA) is a rare hereditary neuropathy, which is associated with defective sensation to noxious stimuli and autonomic …
JK Minde - Acta orthopaedica, 2006 - Taylor & Francis
Previously, the terms congenital insensitivity to pain and congenital indifference to pain were used interchangeably (Jewesbury et al. 1970, McMurray et al. 1950). However, the presence …
CRD Oliveira, VC Paris, RA Pereira… - Revista brasileira de …, 2009 - SciELO Brasil
JUSTIFICATIVA E OBJETIVOS: A insensibilidade congênita a dor e anidrose (ICDA) ou neuropatia hereditária sensorial e autonômica tipo IV (NHSA tipo IV) é neuropatia …
C Suriu, M Khayat, M Weiler, N Kfir, C Cohen… - Clinical …, 2009 - Wiley Online Library
Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV is a rare, autosomal recessive neurologic disorder, characterized by …
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease, characterized by episodes of unexplained fever, anhidrosis, pain insensitivity …