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...

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Detalles Bibliográficos
Autores principales: Tahir, Amber, Tariq, Syed Maaz, Haider, Syed Ali, Hasan, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318104/
https://www.ncbi.nlm.nih.gov/pubmed/30648059
http://dx.doi.org/10.7759/cureus.3524

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318104/
https://www.ncbi.nlm.nih.gov/pubmed/30648059
http://dx.doi.org/10.7759/cureus.3524

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