Skin fragility - plakoglobin deficiency (Q99248): Difference between revisions
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15 August 2026
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Latest revision as of 15:55, 16 August 2026
A rare autosomal recessive skin fragility syndrome due to mutations in the JUP gene which encodes plakoglobin, a protein essential for epidermal integrity. It presents with widespread erosions, sparse woolly hair, nail dystrophy and focal palmoplantar keratoderma.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1145805364 |
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| English | Skin fragility - plakoglobin deficiency |
A rare autosomal recessive skin fragility syndrome due to mutations in the JUP gene which encodes plakoglobin, a protein essential for epidermal integrity. It presents with widespread erosions, sparse woolly hair, nail dystrophy and focal palmoplantar keratoderma. |
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CID11:ID_1145805364
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dki-india-ID_1145805364
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Concluído
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15 August 2026
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