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acral type Peeling skin syndrome

An autosomal recessive genodermatosis characterized by the shedding of the outer epidermis. In the acral type (PSS2), the dorsa of the hands and feet are predominantly affected, and ultrastructural analysis shows separation at the junction between the granular cells and the stratum corneum in the outer epidermis. Mutations in the TGM5 gene have been identified. OMIM: 609796
Also Known As:
Peeling skin syndrome, acral type; Acral peeling skin syndrome; Peeling skin syndrome 2
Networked: 7 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Type 2 von Willebrand Disease
2. Adrenogenital Syndrome
3. Rare Diseases (Rare Disease)
4. Cytochrome-c Oxidase Deficiency
5. Spinocerebellar Ataxias (Spinocerebellar Ataxia)

Experts

1. Akhapkina, Tatiana A: 1 article (07/2019)
2. Aleksakhina, Svetlana N: 1 article (07/2019)
3. Anisimova, Maria O: 1 article (07/2019)
4. Bizin, Ilya V: 1 article (07/2019)
5. Holmatov, Maxim M: 1 article (07/2019)
6. Imyanitov, Evgeny N: 1 article (07/2019)
7. Iyevleva, Aglaya G: 1 article (07/2019)
8. Koloskov, Andrey V: 1 article (07/2019)
9. Kuligina, Ekaterina Sh: 1 article (07/2019)
10. Matsneva, Maria A: 1 article (07/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to acral type Peeling skin syndrome:
1. transglutaminase 5IBA
2. Cystatin AIBA
3. Nonsense Codon (Nonsense Mutation)IBA
4. Proteins (Proteins, Gene)FDA Link
5. Complement C2 (Complement Component 2)IBA
6. Complement System Proteins (Complement)IBA