Acral skin peeling syndrome (Q83638): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 09:00, 15 August 2026
Acral peeling skin syndrome is caused by mutations in the TGM5 gene, the product of which is transglutaminase 5, an enzyme which plays a critical role in the formation of the cornified cell envelope which surrounds keratinocytes in the upper epidermis and is vital to epidermal integrity. Skin peeling is usually evident from birth and is most noticeable on the hands and feet.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1869724137 |
||
| English | Acral skin peeling syndrome |
Acral peeling skin syndrome is caused by mutations in the TGM5 gene, the product of which is transglutaminase 5, an enzyme which plays a critical role in the formation of the cornified cell envelope which surrounds keratinocytes in the upper epidermis and is vital to epidermal integrity. Skin peeling is usually evident from birth and is most noticeable on the hands and feet. |
Statements
CID11:ID_1869724137
0 references
dki-india-ID_1869724137
0 references
Concluído
0 references
13 August 2026
0 references
