Page last updated: 2024-10-15

acetylcarnitine and Hereditary Sensory and Autonomic Neuropathies

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

Acetylcarnitine: An acetic acid ester of CARNITINE that facilitates movement of ACETYL COA into the matrices of mammalian MITOCHONDRIA during the oxidation of FATTY ACIDS.

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-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gago, MF1
Rosas, MJ1
GuimarĂ£es, J1
Ferreira, M1
Vilarinho, L1
Castro, L1
Carpenter, S1

Other Studies

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

ArticleYear
SANDO: two novel mutations in POLG1 gene.
    Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:8

    Topics: Acetylcarnitine; Adult; Coenzymes; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA P

2006