Cargando…
A rare case of congenital aniridia with an unusual run-on mutation in PAX6 gene
Autores principales: | Ratna, Ria, Tibrewal, Shailja, Gour, Abha, Gupta, Reena, Mathur, Umang, Vanita, Vanita |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426074/ https://www.ncbi.nlm.nih.gov/pubmed/35791194 http://dx.doi.org/10.4103/ijo.IJO_433_22 |
Ejemplares similares
-
Clinical and molecular aspects of congenital aniridia – A review of current concepts
por: Tibrewal, Shailja, et al.
Publicado: (2022) -
An unusual twinning moment – A rare occurrence of unilateral congenital dacryocystocele in a pair of monozygotic identical twins
por: Ramesh, Shruthy V, et al.
Publicado: (2022) -
Congenital entropion with progeria: 4 going 40
por: Gupta, Himika, et al.
Publicado: (2022) -
Bilateral buphthalmos with congenital cataract in a floppy infant
por: Jacob, Ninan, et al.
Publicado: (2022) -
A rare case of congenital fibrosis of extra ocular muscles with Kallmann syndrome
por: Yenugandula, Raman, et al.
Publicado: (2022)