Synonyms of Peeling Skin Syndrome- Deciduous Skin
- Familial Continuous Skin Peeling
- Keratolysis Exfoliativa Congenita
- Skin Peeling Syndrome
Disorder Subdivisions
- Acral Peeling Skin Syndrome
General DiscussionPeeling skin syndrome is an extremely rare inherited disorder characterized by continual, spontaneous skin peeling (exfoliation). Other findings may include reddening of the skin (erythema) and itching (pruritus). At least one group working on this disorder distinguishes between a non-inflammatory form called type A and an inflammatory form known as type B. Type B is associated with congenital erythroderma, a condition in which the skin has an intense red color. There is mounting evidence that the inflammatory type B is a variant of Netherton syndrome.
Based on its occurrence in families in which husband and wife are close relatives, peeling skin syndrome is likely to be transmitted as an autosomal recessive genetic trait.
Organizations related to Peeling Skin Syndrome- Foundation for Ichthyosis & Related Skin Types
1364 Welsh Road G2
North Wales PA 19454
Phone #: 215-619-0670
800 #: 800-545-3286
e-mail: [email protected]
Home page: http://www.scalyskin.org
- NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
1 AMS Circle
Bethesda MD 20892-3675
Phone #: 301-495-4484
800 #: 877-226-4267
e-mail: [email protected]
Home page: http://www.niams.nih.gov/Health_Info
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ? (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html