0000000001186912

AUTHOR

M. Laue

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Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study

2010

Background:  Early occurrence of small-fibre neuropathy (SFN) is a common feature of Fabry disease (FD) – an X-linked storage disorder caused by reduced activity of the α-galactosidase A (α-GAL). Although SFN may result from different disorders, the cause is often unclear. Therefore, we investigated the frequency of FD in patients with SFN of unknown aetiology. Methods:  Patients with idiopathic SFN, established by sensory quantitative testing and/or skin biopsy, were examined for mutations in the α-GAL gene. Where mutations in the α-GAL gene were identified, levels of globotriaosylceramide (Gb3) were measured in urine and blood and the α-GAL activity was evaluated. When new mutations were …

Mutationmedicine.medical_specialtyPathologyAlpha-galactosidasemedicine.diagnostic_testbiologybusiness.industryHaplotypeGlobotriaosylceramideEnzyme replacement therapymedicine.diseasemedicine.disease_causeFabry diseaseGastroenterologyPathogenesischemistry.chemical_compoundNeurologychemistryInternal medicineSkin biopsymedicinebiology.proteinNeurology (clinical)businessEuropean Journal of Neurology
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