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

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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Bibliographic Details
Main Authors: Jacopo Pruccoli, Claudio Graziano, Chiara Locatelli, Lucia Maltoni, Hodman Ahmed Sheikh Maye, Duccio Maria Cordelli
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Genes
Subjects:
ring chromosome 10
r10
r(10)
neurology
neuroradiology
magnetic resonance imaging (MRI)
Online Access:https://www.mdpi.com/2073-4425/12/10/1513

Internet

https://www.mdpi.com/2073-4425/12/10/1513

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