19p13.3 Deletion With Polyotia: A Case Report and Literature Review

Mutations at chromosome 19 are rare, and reports in the literature are scarce and clinically variable. This chromosome has a high genetic density, and hence a given deletion can cause distinctive effects on body systems and, in addition, result in a characteristic phenotype.  We report the case of a...

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Detalles Bibliográficos
Autores principales: Silvera Redondo, Carlos, Avendaño Capriles, Camilo Andrés, Fernández Sánchez, David, David Espinosa, Ricardo, Acostamadiedo Marx, Ana Sofía
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680017/
https://www.ncbi.nlm.nih.gov/pubmed/34976455
http://dx.doi.org/10.7759/cureus.19661

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680017/
https://www.ncbi.nlm.nih.gov/pubmed/34976455
http://dx.doi.org/10.7759/cureus.19661

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