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...

وصف كامل

التفاصيل البيبلوغرافية

الحاوية / القاعدة:	Medicina
المؤلفون الرئيسيون:	Laura Cristina Gironi, Francesca Zottarelli, Gianfranco Savoldi, Lucia Dora Notarangelo, Maria Eleonora Basso, Ivana Ferrero, Fabio Timeus, Franca Fagioli, Luigi Maiuri, Enrico Colombo, Paola Savoia
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	MDPI AG 2019-03-01
الموضوعات:	genodermatoses genetic skin disorders pigmentation disorders gray hair syndromes griscelli syndrome congenital hypopigmentary disorders
الوصول للمادة أونلاين:	https://www.mdpi.com/1010-660X/55/3/78