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Fabry disease in the Spanish population: observational study with detection of 77 patients.

Irene VieitezOlga Souto-RodriguezLorena Fernandez-MosqueraBeatriz San MillanSusana TeijeiraJulian Fernandez-MartinFelisa Martinez-SanchezLuis Jose Aldamiz-EchevarriaMonica Lopez-RodriguezCarmen NavarroSaida Ortolano
Published in: Orphanet journal of rare diseases (2018)
Enzymatic screening for Fabry Disease in risk population (2 or more clinical manifestations or family history of the disease) helped to identify undiagnosed patients and unravel the impairment of GLA expression in some subjects with complex haplotypes.
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