Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes

The term congenital hypopigmentary disorders refers to a wide group of heterogeneous hereditary diseases, clinically characterized by inborn pigmentary defects of the iris, hair, and/or skin. They include Gray Hair Syndromes (GHSs), a rare group of autosomal recessive genodermatosis hallmarked by in...

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Detalles Bibliográficos
Autores principales: Gironi, Laura Cristina, Zottarelli, Francesca, Savoldi, Gianfranco, Notarangelo, Lucia Dora, Basso, Maria Eleonora, Ferrero, Ivana, Timeus, Fabio, Fagioli, Franca, Maiuri, Luigi, Colombo, Enrico, Savoia, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473230/
https://www.ncbi.nlm.nih.gov/pubmed/30934652
http://dx.doi.org/10.3390/medicina55030078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473230/
https://www.ncbi.nlm.nih.gov/pubmed/30934652
http://dx.doi.org/10.3390/medicina55030078

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