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Up to: Syndromic disease · Disorder of development or morphogenesis · T-B- severe combined immunodeficiency
DNA ligase IV deficiency
LIG4 syndrome is a hereditary disorder associated with impaired DNA double-strand break repair mechanisms and characterized by microcephaly, unusual facial features, growth and developmental delay, skin anomalies, and pancytopenia, which is associated with combined immunodeficiency (CID).
This condition has no sub-types.