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

Keyphrases

• Combined Immunodeficiency 100%
• Failure to Thrive 100%
• Diagnostic Considerations 100%
• Omenn Syndrome 100%
• Erythroderma 100%
• T Cells 33%
• Mucosal Infection 33%
• Clinical Manifestations 33%
• Anemia 33%
• Peripheral Blood 33%
• Lymph Node 33%
• Eosinophilia 33%
• Autosomal Recessive 33%
• Young Males 33%
• Alopecia 33%
• Lymphadenopathy 33%
• Male Infant 33%
• Lymphocytosis 33%
• Hepatosplenomegaly 33%
• Rare Forms 33%
• Unusual Phenotype 33%

Medicine and Dentistry

• Failure to Thrive 100%
• Erythroderma 100%
• Combined Immunodeficiencies 100%
• Omenn Syndrome 100%
• Infection 33%
• T Cell 33%
• Anemia 33%
• Lymph Node 33%
• Eosinophilia 33%
• Lymphadenopathy 33%
• Alopecia Mucinosa 33%
• Lymphocytosis 33%
• Hepatosplenomegaly 33%
• Autosomal Recessive Inheritance 33%