Multidimensional analysis of clinical symptoms in patients with Fabry's disease

Summary Aim: Fabry’s disease is an X‐linked inherited lysosomal storage disorder caused by the deficient activity of alpha‐galactosidase A. The interrelationships between clinical symptoms in Fabry patients have not yet been fully established. Using cluster and multivariate analysis, the aim of the...

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Veröffentlicht in:	International journal of clinical practice (Esher) 2013-02, Vol.67 (2), p.120-127
Hauptverfasser:	Kaminsky, P., Noel, E., Jaussaud, R., Leguy-Seguin, V., Hachulla, E., Zenone, T., Lavigne, C., Marie, I., Maillot, F., Masseau, A., Serratrice, C., Lidove, O.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age of Onset Biological and medical sciences Brain Diseases - etiology Child Child, Preschool Clinical medicine Errors of metabolism Fabry Disease - complications Female General aspects Hearing Loss - etiology Heart Diseases - etiology Human health and pathology Humans Kidney Diseases - etiology Life Sciences Lipids (lysosomal enzyme disorders, storage diseases) Male Medical sciences Metabolic diseases Metabolic disorders Risk Factors Sex Factors Young Adult
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