Cargando…
Discordant phenotypes in twins with infantile nystagmus
Infantile nystagmus (IN) may result from aetiologies including albinism and FRMD7 mutations. IN has low prevalence, and twins with IN are rare. Whilst discordant presentation has been previously reported for IN, we present for the first time the comprehensive assessment of diagnostically discordant...
Autores principales: | Aamir, Abdullah, Kuht, Helen J., McLean, Rebecca J., Maconachie, Gail D. E., Sheth, Viral, Dawar, Basu, Purohit, Ravi, Sylvius, Nicolas, Hisaund, Michael, Zubcov-Iwantscheff, Alina, Proudlock, Frank A., Gottlob, Irene, Thomas, Mervyn G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854608/ https://www.ncbi.nlm.nih.gov/pubmed/33531592 http://dx.doi.org/10.1038/s41598-021-82368-0 |
Ejemplares similares
-
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
por: Kuht, Helen J, et al.
Publicado: (2020) -
Development and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing
por: Thomas, Mervyn G, et al.
Publicado: (2017) -
Abnormal foveal morphology in carriers of oculocutaneous albinism
por: Kuht, Helen J, et al.
Publicado: (2023) -
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles
por: Thomas, Mervyn G., et al.
Publicado: (2021) -
Can Structural Grading of Foveal Hypoplasia Predict Future Vision in Infantile Nystagmus?: A Longitudinal Study
por: Rufai, Sohaib R., et al.
Publicado: (2020)