Expanding the Neurological Phenotype of Ring Chromosome 10 Syndrome: A Case Report and Review of the Literature

Ring chromosome 10 [r(10)] syndrome is a rare genetic condition, currently described in the medical literature in a small number of case report studies. Typical clinical features include microcephaly, short stature, facial dysmorphisms, ophthalmologic abnormalities and genitourinary malformations. W...

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Detalles Bibliográficos
Autores principales: Pruccoli, Jacopo, Graziano, Claudio, Locatelli, Chiara, Maltoni, Lucia, Sheikh Maye, Hodman Ahmed, Cordelli, Duccio Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535287/
https://www.ncbi.nlm.nih.gov/pubmed/34680908
http://dx.doi.org/10.3390/genes12101513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535287/
https://www.ncbi.nlm.nih.gov/pubmed/34680908
http://dx.doi.org/10.3390/genes12101513

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