Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study.

16q24.3 ANKRD11 adaptive functioning cognitive abilities intellectual disabilities

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
06 Apr 2021
Historique:
received: 04 02 2021
revised: 30 03 2021
accepted: 01 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

KBG syndrome (KBGS) is a rare Mendelian condition caused by heterozygous mutations in

Identifiants

pubmed: 33917340
pii: jcm10071523
doi: 10.3390/jcm10071523
pmc: PMC8038739
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

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Auteurs

Paolo Alfieri (P)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Cristina Caciolo (C)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Giulia Lazzaro (G)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Department of Human Science, LUMSA University of Rome, 00193 Rome, Italy.

Deny Menghini (D)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Francesca Cumbo (F)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Maria Lisa Dentici (ML)

Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Maria Cristina Digilio (MC)

Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Maria Gnazzo (M)

Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Francesco Demaria (F)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Virginia Pironi (V)

Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario A. Gemelli, Catholic University, 00168 Rome, Italy.

Giuseppe Zampino (G)

Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario A. Gemelli, Catholic University, 00168 Rome, Italy.

Antonio Novelli (A)

Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Marco Tartaglia (M)

Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

Stefano Vicari (S)

Department of Neuroscience, Child and Adolescent Psychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Department of Life Sciences and Public Healt, Fondazione Policlinico Universitario A. Gemelli, Catholic University, 00168 Rome, Italy.

Classifications MeSH