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Peeling skin syndrome- Definition, Treatment and Prevention

Definition

Peeling skin syndrome is a group of rare inherited skin disorders characterized by painless, continual, spontaneous skin peeling (exfoliation) due to a separation of the outermost layer of the epidermis (stratum corneum) from the underlying layers. Other findings may include blistering and/or reddening of the skin(erythema) and itching (pruritus).

Peeling skin syndrome in hand

Symptoms may be present from birth or appear in early childhood. Based on the extent of skin involvement, two forms of peeling skin syndrome are recognized: a generalized form involving the entire integument, and an acral form involving only the extremities, and mostly hands and feet.

Generalized peeling skin syndrome may clinically overlap with Netherton syndrome, which is another autosomal recessive skin disorder belonging to the group of congenital ichthyoses, with onset in the neonatal period and infancy.

Types

There are two main types of the generalised Peeling Skin syndrome:

Type A (non-inflammatory) PSS

Type B (inflammatory) PSS

Causes

Your skin is regularly exposed to environmental elements that can irritate and damage it. These include sun, wind, heat, dryness and excessive humidity. Repeated irritation can lead to skin peeling. In babies born past their due date, it’snot unusual for them to experience some painless skin peeling.

Skin peeling can also result from a disease or condition, which may start other than your skin. This type of skin peeling is often by itching. Conditions that may cause skin peeling include:

Symptoms

Some of the symptoms of Peeling skin syndrome:


Symptoms of peeling skin syndrome

Diagnosis

Treatment

Prevention

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