Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Autoimmune lymphoproliferative syndrome type 2 is an autosomal dominant disorder caused by mutations of the CASP10 gene, associated with increased risk of Hodgkin and non-Hodgkin lymphomas.
Lymphoproliferative syndrome
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Autoimmune lymphoproliferative syndrome type 2
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CASP10
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Lymphoproliferative syndrome 1
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X-linked lymphoproliferative syndrome 1
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X-linked lymphoproliferative syndrome 2
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| 1. |
Wang J et al. (1999) Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II. 
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| 2. |
Zhu S et al. (2006) Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome.
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| 3. |
Sneller MC et al. (1997) Clincal, immunologic, and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis.
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