Microcephaly and Chorioretinopathy Relevance as a Differential Diagnosis

Microcephaly and chorioretinopathy are genetic disorders that are inherited in an autosomal recessive manner. The most frequent ocular manifestation is the presence of lacunar atrophy in the retina and choroid. The diagnosis of this condition can be challenging as several potential causes and relate...

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Detalles Bibliográficos
Autores principales: Bayram-Suverza, Mauricio, Torres-Navarro, Karla Alejandra, Hernández-Vázquez, Ángeles Yahel, Ramírez-Estudillo, Juan Abel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417591/
https://www.ncbi.nlm.nih.gov/pubmed/37568951
http://dx.doi.org/10.3390/diagnostics13152588

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417591/
https://www.ncbi.nlm.nih.gov/pubmed/37568951
http://dx.doi.org/10.3390/diagnostics13152588

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