Late-Onset 22q11.2 Deletion Syndrome With Mild Cardiac Phenotype: A Unique Adult Presentation Diagnosed at 45 Years of Age

This case report presents a detailed exploration of an adult-onset 22q11 deletion syndrome, a rare genetic disorder typically diagnosed in children. The report highlights the diagnostic challenges posed by this atypical presentation, emphasizing the need for clinicians to consider such conditions in...

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Detalles Bibliográficos

Autores principales:	Elizondo Plazas, Anasofia, López Uriarte, Graciela Areli, González González, José Gerardo, Rodríguez Gutiérrez, René, Martínez Villarreal, Laura Esther, Treviño Juárez, Ángel Sebastián, González Velázquez, Camilo Daniel
Formato:	Artículo
Lenguaje:	inglés
Publicado:	2023
Materias:	RC Medicina Interna, Psiquiatría, Neurología
Acceso en línea:	http://eprints.uanl.mx/27706/1/434.pdf