Developmental milestones and daily living skills in individuals with Angelman syndrome

被引:2
作者
Sadhwani, Anjali [1 ,2 ]
Powers, Sonya [3 ,11 ]
Wheeler, Anne [3 ]
Miller, Hillary [4 ,12 ]
Potter, Sarah Nelson [3 ]
Peters, Sarika U. [5 ]
Bacino, Carlos A. [6 ]
Skinner, Steven A. [7 ]
Wink, Logan K. [8 ,13 ]
Erickson, Craig A. [8 ]
Bird, Lynne M. [9 ,10 ]
Tan, Wen-Hann [1 ,14 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Psychiat & Behav Serv, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Dept Psychiat & Behav Serv, 300 Longwood Ave, Boston, MA 02115 USA
[3] RTI Int, Res Triangle Pk, NC USA
[4] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[5] Vanderbilt Univ, Sch Med, Nashville, TN USA
[6] Texas Childrens Hosp, Baylor Coll Med, Kleberg Genet Clin, Houston, TX USA
[7] Greenwood Genet Ctr, Greenwood, SC USA
[8] Cincinnati Childrens Hosp Med Ctr, Div Child Psychiat, Cincinnati, OH USA
[9] Univ Calif San Diego, San Diego, CA USA
[10] Rady Childrens Hosp, San Diego, CA USA
[11] Edmentum, Minneapolis, MN USA
[12] Aetna, Hartford, CT USA
[13] Talkiatry Management Serv LLC, New York, NY USA
[14] Harvard Med Sch, Div Genet & Genom, Boston Childrens Hosp, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Child development; Developmental disabilities; Intellectual disability; Activities of Daily Living; ADAPTIVE-BEHAVIOR; PARENTAL RECALL; CHILDREN; PREVALENCE; MUTATIONS; AGE;
D O I
10.1186/s11689-024-09548-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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页数:15
相关论文
共 41 条
[1]   Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes [J].
Beygo, Jasmin ;
Buiting, Karin ;
Ramsden, Simon C. ;
Ellis, Rachael ;
Clayton-Smith, Jill ;
Kanber, Deniz .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 (09) :1326-1340
[2]   An overview of health issues and development in a large clinical cohort of children with Angelman syndrome [J].
Bindels-de Heus, Karen G. C. B. ;
Mous, Sabine E. ;
ten Hooven-Radstaake, Maartje ;
van Iperen-Kolk, Bianca M. ;
Navis, Cindy ;
Rietman, Andre B. ;
ten Hoopen, Leontine W. ;
Brooks, Alice S. ;
Affourtit, Philine ;
Bruggenwirth, Hennie T. ;
Dieleman, Gwen C. ;
Dierckx, Bram ;
Elgersma, Ype ;
ten Hoopen, Leontine W. ;
ten Hooven-Radstaake, Maartje ;
Legerstee, Jeroen S. ;
van der Louw, Elles J. T. M. ;
Moll, Henriette A. ;
Mous, Sabine E. ;
de Nijs, Pieter F. A. ;
Valstar, Marlies J. ;
de Wit, Marie-Claire Y. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (01) :53-63
[3]   Angelman syndrome: review of clinical and molecular aspects [J].
Bird, Lynne M. .
APPLICATION OF CLINICAL GENETICS, 2014, 7 :93-104
[4]   Adaptive behaviour in Angelman syndrome: its profile and relationship to age [J].
Brun Gasca, C. ;
Obiols, J. E. ;
Bonillo, A. ;
Artigas, J. ;
Lorente, I. ;
Gabau, E. ;
Guitart, M. ;
Turk, J. .
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2010, 54 :1024-1029
[5]   Angelman syndrome - insights into a rare neurogenetic disorder [J].
Buiting, Karin ;
Williams, Charles ;
Horsthemke, Bernhard .
NATURE REVIEWS NEUROLOGY, 2016, 12 (10) :584-593
[6]   Angelman syndrome: a review of the clinical and genetic aspects [J].
Clayton-Smith, J ;
Laan, L .
JOURNAL OF MEDICAL GENETICS, 2003, 40 (02) :87-95
[7]   Molecular and Clinical Aspects of Angelman Syndrome [J].
Dagli, A. ;
Buiting, K. ;
Williams, C. A. .
MOLECULAR SYNDROMOLOGY, 2011, 2 (3-5) :100-112
[8]  
Dagli AI., 1998, Angelman Syndrome
[9]   Use of a modified Azrin-Foxx toilet training procedure with individuals with Angelman syndrome [J].
Didden, R ;
Sikkema, SPE ;
Bosman, ITM ;
Duker, PC ;
Curfs, LMG .
JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES, 2001, 14 (01) :64-70
[10]   A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations [J].
Gentile, Jennifer K. ;
Tan, Wen-Hann ;
Horowitz, Lucia T. ;
Bacino, Carlos A. ;
Skinner, Steven A. ;
Barbieri-Welge, Rene ;
Bauer-Carlin, Astrid ;
Beaudet, Arthur L. ;
Bichell, Terry Jo ;
Lee, Hye-Seung ;
Sahoo, Trilochan ;
Waisbren, Susan E. ;
Bird, Lynne M. ;
Peters, Sarika U. .
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, 2010, 31 (07) :592-601