Clinical and Molecular Characterization of a Patient with 15q21.2q22.2 Deletion Syndrome

Ana Claudia Velázquez-Wong,Ruth Ruiz Esparza-Garrido,Miguel Angel Velázquez Flores,Juan Carlos Huicochea-Montiel,Alan Cárdenas-Conejo,Cristian P. Miguez-Muñoz,Araujo-Solís Ma,Fabio Salamanca-Gómez,Diego Arenas Aranda

Clinical and Molecular Characterization of a Patient with 15q21.2q22.2 Deletion Syndrome

2014

Ana Claudia Velázquez-Wong
Ruth Ruiz Esparza-Garrido
Miguel Angel Velázquez Flores
Juan Carlos Huicochea-Montiel
Alan Cárdenas-Conejo
Cristian P. Miguez-Muñoz
Araujo-Solís Ma
Fabio Salamanca-Gómez
Diego Arenas Aranda

We report on a 16-year-old girl with a complex phenotype, including intellectual disability, facial dysmorphisms, and obesity. During her infancy, she presented with weak sucking, global developmental

Keywords:

Molecular biology
Genetics
Biology
Phenotype
Intellectual disability
Weak sucking
Girl
Chromosomal rearrangement
Bioinformatics
Global developmental delay
Breakpoint
deletion syndrome
Chromosomal region

Correction
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