Of 33 children and adolescents (median age 6 years) investigated for learning disability, epilepsy, and motor dysfunction to detect suspected Angelman syndrome (AS), in a study at Goteborg University, Sweden, 23 fulfilled criteria for AS. Distal lower limb spasticity, ataxic like gait with hand flapping, and muscle weakness, milder than findings in most CP, were significantly more frequent in AS than in a comparison group. [1]

Motor Impairments in Angelman Syndrome
DOI: https://doi.org/10.15844/pedneurbriefs-18-4-11 | Journal eISSN: 2166-6482
Language: English
Page range: 32 - 32
Published on: Apr 1, 2004
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2004 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.