Deletion Syndrome 22q11.2: A Systematic Review

22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of the q11.2 region of chromosome 22. It affects one in 4000 live newborns, and among the clinical manifestations that can occur in this syndrome are abnormalities in the parathyroid glands (producing calc...

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Detalles Bibliográficos
Autores principales: Cortés-Martín, Jonathan, Peñuela, Nuria López, Sánchez-García, Juan Carlos, Montiel-Troya, Maria, Díaz-Rodríguez, Lourdes, Rodríguez-Blanque, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406687/
https://www.ncbi.nlm.nih.gov/pubmed/36010058
http://dx.doi.org/10.3390/children9081168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406687/
https://www.ncbi.nlm.nih.gov/pubmed/36010058
http://dx.doi.org/10.3390/children9081168

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