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Transplantační medicína

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Fabry disease

Fabry disease is an X-linked lysosomal storage disease due to a defect in the gene encoding the lysosomal enzyme alpha-galactosidase A (α-Gal A), causing progressive cellular accumulation of the substrate globotriaosylceramide (GL-3) and globo-triaosylsphingosine (lyso-GL-3).

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Fabry disease

Fabry disease is an X-linked lysosomal storage disease due to a defect in the gene encoding the lysosomal enzyme alpha-galactosidase A (α-Gal A), causing progressive cellular accumulation of the substrate globotriaosylceramide (GL-3) and globo-triaosylsphingosine (lyso-GL-3).

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How to diagnose Fabry

Think Fabry, think timely testing first.

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How to diagnose Fabry

Think Fabry, think timely testing first.

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How to diagnose Fabry

Think Fabry, think timely testing first.

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How to diagnose Fabry

Think Fabry, think timely testing first.

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How to diagnose Fabry

Think Fabry, think timely testing first.

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Monitoring disease progression

Think Fabry, think regular profile-based assessments.

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Monitoring disease progression

Think Fabry, think regular profile-based assessments.

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Monitoring disease progression

Think Fabry, think regular profile-based assessments.

Číst více

Monitoring disease progression

Think Fabry, think regular profile-based assessments.

Číst více

Monitoring disease progression

Think Fabry, think regular profile-based assessments.

Číst více