Table 3.
Differential diagnosis of erythroderma presenting in the neonatal period.
| INFECTIONS |
| Staphylococcal scalded skin syndrome (SSSS) |
| Congenital cutaneous candidiasis |
| IMMUNODEFICIENCY |
| Graft-versus-host disease (GvHD) with underlying SCID |
| Omenn’s syndrome |
| ICHTHYOSES |
| Non-syndromic ichthyoses (non-bollous ichthyoses, bollous ichthyoses) |
| Syndromic ichthyoses (Netherton’s syndrome, Conradi–Hünermann syndrome) |
| METABOLIC DISEASES |
| Multiple carboxylase deficiencies |
| Essential fatty acid deficiency |
| DRUGS |
| Ceftriaxone |
| Vancomycin |
| OTHER SKIN PATHOLOGIES |
| Infantile seborrheic dermatitis |
| Atopic dermatitis |
| Psoriasis |
| Cutaneous mastocytosis |