Journal Article

Developmental milestones and daily living skills in individuals with Angelman syndrome

Erickson, Craig A., Sadhwani, Anjali, Bird, Lynne M., Miller, Hillary, Peters, Sarika U., Bacino, Carlos A., Tan, Wen-Hann, Wheeler, Anne, Skinner, Steven A., Potter, Sarah Nelson, Wink, Logan K., Powers, Sonya

2024

Overview

Background Angelman syndrome (AS) is a neurodevelopmental disorder associated with severe global developmental delay. However, the ages at which different developmental skills are achieved in these individuals remain unclear. We seek to determine the probability and the age of acquisition of specific developmental milestones and daily living skills in individuals with AS across the different molecular subtypes, viz. class I deletion, class II deletion, uniparental disomy, imprinting defect, and UBE3A variants. Methods Caregivers participating in a longitudinal multicenter Angelman Syndrome Natural History Study completed a questionnaire regarding the age at which their children achieved specific developmental milestones and daily living skills. The Cox Proportional Hazard model was applied to analyze differences in the probability of achievement of skills at various ages among five molecular subtypes of AS. Results Almost all individuals, regardless of molecular subtype, were able to walk with support by five years of age. By age 15, those with a deletion had at least a 50% probability of acquiring 17 out of 30 skills compared to 25 out of 30 skills among those without a deletion. Overall, fine and gross motor skills such as holding and reaching for small objects, sitting, and walking with support were achieved within a fairly narrow range of ages, while toileting, feeding, and hygiene skills tend to have greater variability in the ages at which these skills were achieved. Those without a deletion had a higher probability (25–92%) of achieving daily living skills such as independently toileting and dressing compared to those with a deletion (0–13%). Across all molecular subtypes, there was a low probability of achieving independence in bathing and brushing teeth. Conclusion Individuals with AS without a deletion are more likely to achieve developmental milestones and daily living skills at an earlier age than those with a deletion. Many individuals with AS are unable to achieve daily living skills necessary for independent self-care.

• Publisher: BioMed Central,BioMed Central Ltd,BMC
• Subject: Activities of Daily Living / Adolescent / Adult / Analysis / Angelman Syndrome - complications / Angelman Syndrome - genetics / Angelman Syndrome - physiopathology / Biomedical and Life Sciences / Biomedicine / Child / Child development / Child Development - physiology / Child, Preschool / Developmental disabilities / Developmental Disabilities - etiology / Female / Human Genetics / Humans / Hygiene / Infant / Intellectual disability / Life skills / Longitudinal Studies / Male / Medical research / Medicine, Experimental / Motor Skills - physiology / Neurology / Neuropsychology / Neurosciences / Pediatrics / Psychiatry / Young Adult