Immune dysfunction with T-cell inactivation due to calcium entry defect 2
Immunodeficiency-10 is an autosomal recessive primary immunodeficiency characterized by onset of recurrent infections in childhood due to defective T- and NK-cell function, although the severity is variable. Affected individuals may also have hypotonia, hypohidrosis, or dental enamel hypoplasia consistent with amelogenesis imperfecta.
NIH genetic and rare disease info[edit source]
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 is a rare disease.
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