Publication Date
| In 2025 | 0 |
| Since 2024 | 0 |
| Since 2021 (last 5 years) | 0 |
| Since 2016 (last 10 years) | 0 |
| Since 2006 (last 20 years) | 1 |
Descriptor
| Age Differences | 1 |
| Athletes | 1 |
| Case Studies | 1 |
| Child Development | 1 |
| Children | 1 |
| Data Analysis | 1 |
| Disabilities | 1 |
| Evaluation Methods | 1 |
| Infants | 1 |
| Motor Development | 1 |
| Seizures | 1 |
| More ▼ | |
Source
| Developmental Medicine &… | 1 |
Author
| Boggs, Niki | 1 |
| Brashear, Allison | 1 |
| Hill, Deborah F. | 1 |
| Light, Laney S. | 1 |
| McCall, W. Vaughn | 1 |
| Mink, Jonathan W. | 1 |
| Morrison, Leslie | 1 |
| Ozelius, Laurie J. | 1 |
| Snively, Beverly | 1 |
| Stacy, Mark A. | 1 |
| Sweadner, Kathleen J. | 1 |
| More ▼ | |
Publication Type
| Journal Articles | 1 |
| Reports - Descriptive | 1 |
Education Level
| Early Childhood Education | 1 |
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Peer reviewed
Direct linkBrashear, Allison; Mink, Jonathan W.; Hill, Deborah F.; Boggs, Niki; McCall, W. Vaughn; Stacy, Mark A.; Snively, Beverly; Light, Laney S.; Sweadner, Kathleen J.; Ozelius, Laurie J.; Morrison, Leslie – Developmental Medicine & Child Neurology, 2012
We report new clinical features of delayed motor development, hypotonia, and ataxia in two young children with mutations (R756H and D923N) in the "ATP1A3" gene. In adults, mutations in "ATP1A3" cause rapid-onset dystonia-Parkinsonism (RDP, DYT12) with abrupt onset of fixed dystonia. The parents and children were examined and videotaped, and…
Descriptors: Athletes, Sports Medicine, Motor Development, Seizures
