Abstract
Neuropathy is a cause of significant disability in patients with Fabry disease, yet its diagnosis is difficult. In this study we compared the novel noninvasive techniques of corneal confocal microscopy (CCM) to quantify small-fiber pathology, and non-contact corneal aesthesiometry (NCCA) to quantify loss of corneal sensation, with established tests of neuropathy in patients with Fabry disease. Ten heterozygous females with Fabry disease not on enzyme replacement therapy (ERT), 6 heterozygous females, 6 hemizygous males on ERT, and 14 age-matched, healthy volunteers underwent detailed quantification of neuropathic symptoms, neurological deficits, neurophysiology, quantitative sensory testing (QST), NCCA, and CCM. All patients with Fabry disease had significant neuropathic symptoms and an elevated Mainz score. Peroneal nerve amplitude was reduced in all patients and vibration perception threshold was elevated in both male and female patients on ERT. Cold sensation (CS) threshold was significantly reduced in both male and female patients on ERT (P <0.02), but warm sensation (WS) and heat-induced pain (HIP) were only significantly increased in males onERT (P
Original language | English |
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Pages (from-to) | 976-984 |
Number of pages | 8 |
Journal | Muscle and Nerve |
Volume | 40 |
Issue number | 6 |
DOIs | |
Publication status | Published - Dec 2009 |
Keywords
- Corneal confocal microscopy
- Corneal nerves
- Fabry disease
- Neurodegeneration
- Neuropathy small fibers