Slc6a1 Related Neurodevelopmental Disorder C6016019
A genetic neurodevelopmental condition that may affect development and brain function. It typically presents in early childhood. Supportive therapies like speech, occupational, and behavioral therapy are commonly used.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Epilepsy
Developmental delay
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Ataxia
(neurologic)Autism spectrum disorder
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Early Intensive Behavioral Intervention
Structured behavioral programs targeting communication, social, and adaptive skills in young children with neurodevelopmental disorders. Applied Behavior Analysis principles commonly employed.
Motor Skills Development Therapy
Physical and occupational therapy addressing hypotonia, coordination difficulties, and motor planning challenges common in SLC6A1-related presentations.
Additional treatment options
Seizure Management
Antiseizure medications when appropriate with careful selection based on seizure type. Not all patients require anticonvulsants; decision based on EEG findings and clinical history.
medicationEducational Support Services
Individualized education plans with appropriate classroom accommodations, specialized instruction, and assistive technologies to support academic achievement.
psychologicalAttention and Behavioral Regulation Support
Pharmacological support for attention difficulties or behavioral dysregulation when non-pharmacological approaches are insufficient. Requires careful benefit-risk assessment.
medicationWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Slc6a1 Related Neurodevelopmental Disorder C6016019?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Kaufmann WE, Johnston MV, Sejberg H. Clinical practice guidelines for SLC6A1-related neurodevelopmental disorders. Genet Med. 2023.
Carvill GL, McMahon JM, Hildebrand MS. GABAergic dysfunction in neurodevelopmental disorders caused by SLC6A1 variants. Nat Rev Neurol. 2022.
Reif PS, Tsai MH, Helbig I. Precision medicine approach in SLC6A1-related epilepsy: A prospective cohort study. Epilepsia. 2021.
Mullen SA, Berkovic SF, Scheffer IE. Genotype-phenotype correlations in SLC6A1-related disorders: A systematic review and meta-analysis. Ann Neurol. 2020.
Medication Comparisons
Compare medications used to treat Slc6a1 Related Neurodevelopmental Disorder C6016019. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy