Publication Date
| In 2026 | 0 |
| Since 2025 | 0 |
| Since 2022 (last 5 years) | 0 |
| Since 2017 (last 10 years) | 0 |
| Since 2007 (last 20 years) | 2 |
Descriptor
| Drug Therapy | 3 |
| Epilepsy | 3 |
| Genetic Disorders | 3 |
| Adolescents | 2 |
| Child Development | 2 |
| Children | 2 |
| Seizures | 2 |
| Adults | 1 |
| Age Differences | 1 |
| Behavior Problems | 1 |
| Biology | 1 |
| More ▼ | |
Author
| Battaglia, Agatino | 1 |
| Blume, Warren T. | 1 |
| Carey, John C. | 1 |
| Fedoroff, J. Paul | 1 |
| Filippi, Tiziana | 1 |
| Miodrag, Nancy | 1 |
| Richards, Deborah A. | 1 |
| South, Sarah T. | 1 |
| Watson, Shelley Lynn | 1 |
Publication Type
| Journal Articles | 3 |
| Reports - Research | 2 |
| Reports - Descriptive | 1 |
Education Level
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Watson, Shelley Lynn; Richards, Deborah A.; Miodrag, Nancy; Fedoroff, J. Paul – Intellectual and Developmental Disabilities, 2012
Specific genetic syndromes affect individuals' sexual development, experiences, and fertility. Individuals with specific syndromes can also display inappropriate sexual behavior resulting from vulnerabilities presented by their genetic makeup. Using clinical case studies, we discuss the specific impact that Down, Prader-Willi, and Williams…
Descriptors: Sexuality, Sex Education, Adolescents, Intimacy
Battaglia, Agatino; Filippi, Tiziana; South, Sarah T.; Carey, John C. – Developmental Medicine & Child Neurology, 2009
To define the spectrum of epilepsy in Wolf-Hirschhorn syndrome (WHS) better, we studied 87 patients (54 females, 33 males; median age 5.6 years; age range 1-25.6 years) with confirmed 4p16.3 deletion. On the basis of clinical charts, we retrospectively analyzed the evolution of the electroencephalogram (EEG) findings and seizures. Epilepsy…
Descriptors: Age Differences, Epilepsy, Seizures, Identification
Blume, Warren T. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
Lennox-Gastaut (L-G) syndrome is an intractable generalized epilepsy of childhood onset, associated with spike waves at a slow rate and paroxysmal fast activity. These epileptiform discharge patterns are thought to reflect excessive neocortical excitability and arise from neuronal and synaptic features peculiar to the immature central nervous…
Descriptors: Seizures, Brain, Social Isolation, Cognitive Development

Peer reviewed
Direct link
