Conditions / Skin
peeling skin syndrome 1
info · Skin
A peeling skin syndrome that has_material_basis_in homozygous mutation in the CDSN gene on chromosome 6p21.33.
Signs and symptoms
- Increased total eosinophil count
- Increased circulating IgE concentration
- Scaling skin
- Erythroderma
- Pruritus
- Cleavage at junction of stratum corneum and stratum granulosum
- Brittle hair
- Palmoplantar hyperhidrosis
- Asthma
- Onycholysis
Also known as: PSS1; generalized inflammatory peeling skin syndrome; inflammatory peeling skin syndrome; peeling skin syndrome type B