Xp21 DNA microdeletion syndrome in a Chinese family: clinical features show retinitis pigmentosa and chronic granuloma
This study suggests that genetic testing is essential for a definitive diagnosis, which should better assist physicians in prediction, diagnosis, genetic counseling, and guidance for Xp21 DNA microdeletion syndrome.
Source: Frontiers in Genetics - Category: Genetics & Stem Cells Source Type: research
More News: China Health | Genetics | Microdeletion Syndromes | Rare Diseases | Retinitis Pigmentosa | Study