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Ichthyosis Congenita, Harlequin Type: A Fatal Case Report
Harlequin baby is rare and it is the most severe kind of congenital ichthyosis. It manifests as severely keratinized skin with an autosomal recessive inheritance. Incidence of this disease is 1 in 300,000 live births. We report a new case of harlequin ichthyosis (HI) from Pakistan to contribute to t...
Salvato in:
| Pubblicato in: | Cureus |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cureus
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6318104/ https://ncbi.nlm.nih.gov/pubmed/30648059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.3524 |
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