multiple parapelvic cysts in fabry disease

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ID: 206052
2016
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Abstract
Fabry disease is an inherited, X-linked lysosomal storage disorder caused by deficiency of the enzyme alpha galactosidase A (alpha-GLA A), which leads to glycosphingolipid accumulation, mainly globotriaosylceramide, in tissues. Disease prevalence and the index of suspicion are both low, which tends to result in delayed diagnosis and treatment. We present the case of a male Fabry disease patient who manifested no angiokeratoma lesions but presented multiple parapelvic cysts and renal failure. The genetic study revealed an alpha-GLA A gene mutation that had not been recorded in the mutations registry. The de novo mutation was not found in his relatives and it was not transmitted to his offspring. The large number and peculiar appearance of the parapelvic cysts led to the diagnosis.
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azancot2016nefrologamultiple Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;María A. Azancot;Josefa Vila;Carmen Domínguez;Xavier Serres;Eugenia Espinel
Journal demiryolu mühendisliği
Year 2016
DOI
10.1016/j.nefroe.2016.06.004
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