Reticular dysgenesis
MONDO:0009973Reticular dysgenesis is the most severe form of severe combined immunodeficiency (SCID) and is characterized by bilateral sensorineural deafness and a lack of innate and adaptive immune functions leading to fatal septicemia within days after birth if not treated.
Also known as: AK2 deficiency, De Vaal disease, SCID with leukopenia, congenital aleukocytosis, generalised haematopoietic hypoplasia, generalized hematopoietic hypoplasia, reticular dysgenesis, severe combined immunodeficiency with leukopenia
3 clinical trials for this condition and its sub-types, 1 tagged with Reticular dysgenesis itself.
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Sub-types of Reticular dysgenesis
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Immunoerythromyeloid hypoplasia 0 trials