Literature DB >> 6154886

Congenital insensitivity to pain with anhidrosis.

E Rafel, R Alberca, J Bautista, M Navarrete, J Lazo.   

Abstract

A nine-year-old child presented with congenital insensitivity to pain and anhidrosis. Quantitative studies and electron microscopy of the cutaneous branch of the radial nerve revealed almost complete absence of small myelinated and unmyelinated fibers and a disproportionate number of nerve fibers with a diameter of 6-10 micrometers. A grouping of both type 1 and type 2 muscle fibers was also seen. We suggest that this disease entity is not caused by a hereditary sensory neuropathy, but rather that it derives from a developmental defect.

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Year:  1980        PMID: 6154886     DOI: 10.1002/mus.880030305

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  7 in total

1.  Norepinephrine deficiency with normal blood pressure control in congenital insensitivity to pain with anhidrosis.

Authors:  Lucy Norcliffe-Kaufmann; Stuart D Katz; Felicia Axelrod; Horacio Kaufmann
Journal:  Ann Neurol       Date:  2015-03-13       Impact factor: 10.422

2.  Eccrine sweat glands are not innervated in hereditary sensory neuropathy type IV. An electron-microscopic study.

Authors:  J Langer; H H Goebel; S Veit
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

Review 3.  Molecular genetics of hereditary sensory neuropathies.

Authors:  Michaela Auer-Grumbach; Barbara Mauko; Piet Auer-Grumbach; Thomas R Pieber
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

4.  Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.

Authors:  S Mardy; Y Miura; F Endo; I Matsuda; L Sztriha; P Frossard; A Moosa; E A Ismail; A Macaya; G Andria; E Toscano; W Gibson; G E Graham; Y Indo
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

5.  Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Authors:  Beyhan Tüysüz; Fatih Bayrakli; Michael L DiLuna; Kaya Bilguvar; Yasar Bayri; Cengiz Yalcinkaya; Aysegul Bursali; Elif Ozdamar; Baris Korkmaz; Christopher E Mason; Ali K Ozturk; Richard P Lifton; Matthew W State; Murat Gunel
Journal:  Neurogenetics       Date:  2008-03-06       Impact factor: 2.660

6.  Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort.

Authors:  G L Davidson; S M Murphy; J M Polke; M Laura; M A M Salih; F Muntoni; J Blake; S Brandner; N Davies; R Horvath; S Price; M Donaghy; M Roberts; N Foulds; G Ramdharry; D Soler; M P Lunn; H Manji; M B Davis; H Houlden; M M Reilly
Journal:  J Neurol       Date:  2012-08       Impact factor: 4.849

Review 7.  Independent evolution of pain insensitivity in African mole-rats: origins and mechanisms.

Authors:  Ewan St John Smith; Thomas J Park; Gary R Lewin
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2020-03-23       Impact factor: 1.836

  7 in total

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