Cargando…
Cortical Visual Impairment in CDKL5 Deficiency Disorder
BACKGROUND: CDKL5 deficiency disorder (CDD) is a developmental encephalopathy caused by pathogenic variants in the gene cyclin-dependent kinase-like 5. Cerebral visual impairment (CVI) is frequent in patients with CDD. In addition to being recognized as a specific feature of the pathology, it has be...
Autores principales: | Quintiliani, Michela, Ricci, Daniela, Petrianni, Maria, Leone, Simona, Orazi, Lorenzo, Amore, Filippo, Gambardella, Maria Luigia, Contaldo, Ilaria, Veredice, Chiara, Perulli, Marco, Musto, Elisa, Mercuri, Eugenio Maria, Battaglia, Domenica Immacolata |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825365/ https://www.ncbi.nlm.nih.gov/pubmed/35153983 http://dx.doi.org/10.3389/fneur.2021.805745 |
Ejemplares similares
-
Visual Function in Children with GNAO1-Related Encephalopathy
por: Gambardella, Maria Luigia, et al.
Publicado: (2023) -
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation
por: Perulli, Marco, et al.
Publicado: (2022) -
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report
por: Sprovieri, Teresa, et al.
Publicado: (2019) -
Visual Function and Ophthalmological Findings in CHARGE Syndrome: Revision of Literature, Definition of a New Clinical Spectrum and Genotype Phenotype Correlation
por: Onesimo, Roberta, et al.
Publicado: (2021) -
Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations
por: Battaglia, Domenica I., et al.
Publicado: (2021)