Omenn syndrome is
High-Yield Explanation
Omenn syndrome is an autosomal recessive form of severe combined immunodeficiency (SCID) characterized by erythroderma (skin redness), desquamation (peeling skin), alopecia (hair loss), chronic diarrhea, failure to thrive, lymphadenopathy (enlarged lymph nodes ), eosinophilia, hepatosplenomegaly , and elevated serum Ref Harrison20th edition pg 1278