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What is Neonatal and Infantile Erythroderma Diagnosis about?

Neonatal and infantile erythroderma presents a diagnostic and therapeutic challenge as it can be caused by numerous underlying conditions. Differential diagnosis is a multi-step process involving clinical assessment, family history, and laboratory tests. Delay in establishing the correct diagnosis can prove fatal, especially if the underlying cause is an immunodeficiency disorder. Histology and additional testing can help distinguish between potential causes such as infections, genetic disorders, or immune

Author

Jessica Christiana Putri

Language

EN