Dyschromatosis symmetrica hereditaria: Report of a sporadic case in a Nigerian child
Dyschromatosissymmetricahereditaria (DSH) is one of a group of reticulate pigment disorders of the skin. It is a rare autosomal dominantly inherited genodermatosis, presenting as mottled admixtures of hypopigmented and hyperpigmented macules on the dorsa of the extremities. It is predominantly fou...
Furkejuvvon:
| Váldodahkkit: | , , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Paediatric Association of Nigeria
2024-07-01
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| Ráidu: | Nigerian Journal of Paediatrics |
| Fáttát: | |
| Liŋkkat: | https://www.njpaediatrics.com/index.php/njp/article/view/321 |
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