Lenz microphthalmia syndrome in neurosurgical practice: a case report and review of the literature

Lenz microphthalmia syndrome (LMS) is an allelic X-linked syndrome correlated to a null mutation of B cell lymphoma (BCL-6) corepressor (BCOR) gene, which is essential in the early embryonic development. Phenotypically, this rare hereditary syndrome is characterized by microphthalmia/anophthalmia an...

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Detalles Bibliográficos
Autores principales: Monticelli, Matteo, De Marco, Raffaele, Garbossa, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342332/
https://www.ncbi.nlm.nih.gov/pubmed/33491151
http://dx.doi.org/10.1007/s00381-020-05035-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342332/
https://www.ncbi.nlm.nih.gov/pubmed/33491151
http://dx.doi.org/10.1007/s00381-020-05035-1

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