DefinitionThis section has been translated automatically.
Clinical special cases of disease patterns that may be associated with erythroderma in newborns and young infants. S.u. Erythrodermia in newborns and infants.
Differential diagnosisThis section has been translated automatically.
Differential diagnosis of erythroderma in newborns and young infants.
- Infections:
- Staphylococcal Scalded Skin Syndrome
- Candidosis, congenital cutaneous
- shock syndrome, toxic
- Neonatal toxic-shock-like exanthematous disease.
- Immunodeficiency syndromes:
- Primary T-cellular immunodeficiencies (e.g. Omenn syndrome)
- Graft-versus-host disease, acute.
- Ichthyosis:
- Non-bullous ichtyosiform erythroderma (Erythrodermia congenitalis ichthyosiformis nonbullosa)
- Bullous congenital erythroderma ( Erythrodermia congenitalis ichthyosiformis bullosa)
- Netherton Syndrome
- Chondrodysplasia punctata (Conradi-Hünermann syndrome).
- Metabolic diseases:
- Deficiency of essential fatty acids
- multiple carboxylase deficiency
- Fibrosis, cystic (mucoviscidosis).
- Drug-induced:
- Other:
Recommended articles
Outgoing links (19)
Atopic dermatitis (overview); Candidosis, congenital cutaneous; Carboxylase defect, multiple; Ceftriaxone; Chondrodysplasia punctata; Diffuse cutaneous mastocytosis; Epidermolytic ichthyosis; Erythrodermia; Fibrosis cystic; Graft-versus-host disease acute; ... Show allDisclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
Prof. Dr. med. Peter Altmeyer