Hepatic veno-occlusive disease - immunodeficiency syndrome
**Definition:** Hepatic veno-occlusive disease - immunodeficiency syndrome is characterised by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centres, absent tissue plasma cells and hepatic veno-occlusive disease.
**Long definition:** This syndrome is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Prevalence at birth is 1/2 500 in the Lebanese population, 25 cases having been described in a 30-year period. Mutations in the gene coding PML nuclear body protein Sp110 were found to be responsible for this association. Transmission is autosomal recessive. Mortality reaches 85% if the syndrome remains unrecognised and untreated.
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No cross-system equivalences mapped for this node.