Cargando…
Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report
BACKGROUND: Peters plus syndrome (PPS) is a combination of congenital Peters anomaly and systemic abnormalities. It is inherited most commonly in an autosomal recessive pattern with homozygous B3GLCT mutations. Ocular findings consist predominantly anterior segment abnormalities without posterior se...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092513/ https://www.ncbi.nlm.nih.gov/pubmed/32204707 http://dx.doi.org/10.1186/s12886-020-01380-6 |