Page last updated: 2024-11-02

perhexiline and Hereditary Sensory and Autonomic Neuropathies

perhexiline has been researched along with Hereditary Sensory and Autonomic Neuropathies in 1 studies

Perhexiline: 2-(2,2-Dicyclohexylethyl)piperidine. Coronary vasodilator used especially for angina of effort. It may cause neuropathy and hepatitis.

Hereditary Sensory and Autonomic Neuropathies: A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mussini, JM1
Guillemot, A1
Mussini-Montpellier, J1

Other Studies

1 other study available for perhexiline and Hereditary Sensory and Autonomic Neuropathies

ArticleYear
[Contribution of neuromuscular biopsy in cardiovascular diseases].
    Annales de cardiologie et d'angeiologie, 1979, Volume: 28, Issue:6

    Topics: Biopsy; Cardiovascular Diseases; Diagnosis; Hereditary Sensory and Autonomic Neuropathies; Humans; M

1979