KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patients.


Journal

European journal of human genetics : EJHG
ISSN: 1476-5438
Titre abrégé: Eur J Hum Genet
Pays: England
ID NLM: 9302235

Informations de publication

Date de publication:
11 2022
Historique:
received: 10 02 2022
accepted: 26 07 2022
revised: 26 05 2022
pubmed: 16 8 2022
medline: 4 11 2022
entrez: 15 8 2022
Statut: ppublish

Résumé

Genetic variants in Ankyrin Repeat Domain 11 (ANKRD11) and deletions in 16q24.3 are known to cause KBG syndrome, a rare syndrome associated with craniofacial, intellectual, and neurobehavioral anomalies. We report 25 unpublished individuals from 22 families with molecularly confirmed diagnoses. Twelve individuals have de novo variants, three have inherited variants, and one is inherited from a parent with low-level mosaicism. The mode of inheritance was unknown for nine individuals. Twenty are truncating variants, and the remaining five are missense (three of which are found in one family). We present a protocol emphasizing the use of videoconference and artificial intelligence (AI) in collecting and analyzing data for this rare syndrome. A single clinician interviewed 25 individuals throughout eight countries. Participants' medical records were reviewed, and data was uploaded to the Human Disease Gene website using Human Phenotype Ontology (HPO) terms. Photos of the participants were analyzed by the GestaltMatcher and DeepGestalt, Face2Gene platform (FDNA Inc, USA) algorithms. Within our cohort, common traits included short stature, macrodontia, anteverted nares, wide nasal bridge, wide nasal base, thick eyebrows, synophrys and hypertelorism. Behavioral issues and global developmental delays were widely present. Neurologic abnormalities including seizures and/or EEG abnormalities were common (44%), suggesting that early detection and seizure prophylaxis could be an important point of intervention. Almost a quarter (24%) were diagnosed with attention deficit hyperactivity disorder and 28% were diagnosed with autism spectrum disorder. Based on the data, we provide a set of recommendations regarding diagnostic and treatment approaches for KBG syndrome.

Identifiants

pubmed: 35970914
doi: 10.1038/s41431-022-01171-1
pii: 10.1038/s41431-022-01171-1
pmc: PMC9626563
doi:

Substances chimiques

Repressor Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1244-1254

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM133408
Pays : United States

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Lily Guo (L)

Department of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA.

Jiyeon Park (J)

Department of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA.

Edward Yi (E)

Department of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA.

Elaine Marchi (E)

Department of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA.

Tzung-Chien Hsieh (TC)

Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.

Yana Kibalnyk (Y)

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.
Department of Cell Biology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.

Yolanda Moreno-Sáez (Y)

Medical Genetic Unit, Sistemas Genómicos, Valencia, Spain.

Saskia Biskup (S)

CeGaT GmbH, Praxis für Humangenetik Tübingen, Tübingen, Germany.

Oliver Puk (O)

CeGaT GmbH, Praxis für Humangenetik Tübingen, Tübingen, Germany.

Carmela Beger (C)

MVZ Labor Krone GbR, Filialpraxis für Humangenetik, Bielefeld, Germany.

Quan Li (Q)

Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, M5G2C1, Canada.

Kai Wang (K)

Raymond G. Perelman Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA.

Anastassia Voronova (A)

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.
Department of Cell Biology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.

Peter M Krawitz (PM)

Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.

Gholson J Lyon (GJ)

Department of Human Genetics, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA. gholsonjlyon@gmail.com.
George A. Jervis Clinic, NYS Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY, 10314, USA. gholsonjlyon@gmail.com.
Biology PhD Program, The Graduate Center, The City University of New York, New York, NY, USA. gholsonjlyon@gmail.com.

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