Frontiers in Psychiatry (Feb 2024)
Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports
- Federica Alice Maria Montanaro,
- Alessandra Mandarino,
- Viola Alesi,
- Charles Schwartz,
- Daniela Judith Claps Sepulveda,
- Cindy Skinner,
- Michael Friez,
- Gabriele Piccolo,
- Antonio Novelli,
- Ginevra Zanni,
- Maria Lisa Dentici,
- Stefano Vicari,
- Paolo Alfieri
Affiliations
- Federica Alice Maria Montanaro
- Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Alessandra Mandarino
- Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Viola Alesi
- Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy
- Charles Schwartz
- Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI, United States
- Daniela Judith Claps Sepulveda
- Neurology Unit, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Cindy Skinner
- Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States
- Michael Friez
- Greenwood Genetic Center, Gregor Mendel Circle, Greenwood, SC, United States
- Gabriele Piccolo
- Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Antonio Novelli
- Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, Rome, Italy
- Ginevra Zanni
- Unit of Muscular and Neurodegenerative Disorders, Unit of Developmental Neurology, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Maria Lisa Dentici
- Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Stefano Vicari
- Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- Paolo Alfieri
- Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
- DOI
- https://doi.org/10.3389/fpsyt.2024.1375954
- Journal volume & issue
-
Vol. 15
Abstract
No abstracts available.Keywords
- PTCHD1 gene
- intellectual disability
- autism spectrum disorder
- rare genetic syndrome
- cognitive-behavioral phenotype