Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thrive

Medicine and Dentistry

• Combined Immunodeficiency 100%
• Erythroderma 66%
• Omenn Syndrome 66%
• Infant 66%
• Failure to Thrive 66%
• Phenotype 33%
• Lymph Node 33%
• Diagnosis 33%
• Lymphadenopathy 33%
• Infection 33%
• Autosomal Recessive Inheritance 33%
• Eosinophilia 33%
• Anemia 33%
• Alopecia Mucinosa 33%
• Hepatosplenomegaly 33%
• Lymphocytosis 33%
• T Cell 33%
• Male 33%
• Skin 33%
• Patient 33%
• Blood 33%