O'Donnel-Luria-Rodan Syndrome: New gene variant identified in Romania (A case report)

O'Donnel-Luria-Rodan (ODLURO) syndrome is a neurodevelopmental disorder with autosomal dominant inheritance. It appears more frequently in males during the first decade of life and is associated with developmental delay, low intelligence quotient, autism spectrum disorder-like behavior, epileps...

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Detalles Bibliográficos
Autores principales: Cătană, Andreea, Kutasi, Enikő, Cuzmici-Barabaș, Zina, Militaru, Diana, Iordănescu, Irina, Militaru, Mariela Sanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016787/
https://www.ncbi.nlm.nih.gov/pubmed/35481221
http://dx.doi.org/10.3892/etm.2022.11294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016787/
https://www.ncbi.nlm.nih.gov/pubmed/35481221
http://dx.doi.org/10.3892/etm.2022.11294

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