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Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Early diagnosis and treatment are crucial for complex medical conditions.

Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

IVIG therapy was linked to hair regrowth in two patients with hair loss, but it's not recommended due to its risks and costs.