Atypical Cyanotic Breath-Holding Spells in an Infant With 16p11.2 Microdeletion Syndrome
Author:
Affiliation:
1. University of South Alabama, Mobile, AL, USA
Publisher
SAGE Publications
Subject
Pediatrics, Perinatology, and Child Health
Link
http://journals.sagepub.com/doi/pdf/10.1177/0009922817717328
Reference18 articles.
1. Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations
2. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
3. Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome
4. Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications
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2. Health supervision for children and adolescents with 16p11.2 deletion syndrome;Molecular Case Studies;2023-12
3. Evaluation of the Predictors of Breath Holding Spell (BHS) in under 5-Year-Old Children in Iran: A Hospital-Based Case-Control Study;INT J PEDIATR-MASSHA;2021
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