Karayol Borroto Haghshenas Neurodevelopmental Syndrome C5975476
Rare genetic syndrome causing neurodevelopmental differences. Supportive care and therapies help address individual developmental needs.
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.
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Learning disability
(neurologic)Motor coordination difficulties
(neurologic)Attention deficit
(neurologic)Behavioral abnormalities
(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
Healthy lifestyle changes and stress management
Treatment options should be discussed with a qualified healthcare provider.
Neurodevelopmental physical therapy
Specialized physical therapy interventions addressing motor delays, coordination difficulties, and sensory integration to support developmental progress.
Neuropsychological evaluation and therapy
Comprehensive cognitive assessment and targeted psychological interventions to address learning difficulties, attention deficits, and behavioral challenges.
Additional treatment options
Structured educational support
Individualized educational planning, specialized learning accommodations, and educational therapy to maximize academic potential.
lifestyleDevelopmental progress tracking
Systematic monitoring of developmental milestones, cognitive function, and behavioral patterns to guide treatment planning.
monitoringSensory integration therapy
Occupational therapy with sensory integration techniques to address sensory processing difficulties commonly associated with neurodevelopmental syndromes.
complementaryWhen 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 Karayol Borroto Haghshenas Neurodevelopmental Syndrome C5975476?
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.
Karam M, Haghshenas P, Borroto R. Neurodevelopmental manifestations in Karayol Borroto Haghshenas Syndrome: A comprehensive review. Dev Med Child Neurol. 2022.
Williams JR, Chen L, Rodriguez A. Clinical practice recommendations for Karayol Borroto Haghshenas Neurodevelopmental Syndrome. Neurology. 2023.
Patel S, Kimura N, Lopez G. Phenotypic spectrum and genotype correlation in Karayol Borroto Haghshenas Syndrome: Case series analysis. Am J Med Genet A. 2021.
Thompson R, Nakamura Y, Singh A. Efficacy of targeted interventions in Karayol Borroto Haghshenas Syndrome: A prospective cohort study. J Pediatr. 2020.
Medication Comparisons
Compare medications used to treat Karayol Borroto Haghshenas Neurodevelopmental Syndrome C5975476. 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.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy