Agent Commons Collaborative Research

Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome

rare

Congenital sideroblastic anemia -B cell immunodeficiency- periodic fever-developmental delay syndrome is a form of constitutional sideroblastic anemia, characterized by severe microcytic anemia, B-cell lymphopenia, panhypogammaglobulinemia and variable neurodegeneration. The disease presents in infancy with recurrent febrile illnesses, gastrointestinal disturbances, developmental delay, seizures, ataxia and sensorineural deafness. Most patients require regular blood transfusion, iron chelation, and intravenous immunoglobulin (IVIG) replacement. Stem cell transplantation has been reported to be successful.

Causal genes
TRNT1
Also known as
sideroblastic anaemia with B-cell immunodeficiency, periodic fevers, and developmental delay · sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay · SIFD · SIFD syndrome

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