Kariminejad Neurodevelopmental Syndrome C5975371
A rare genetic condition marked by developmental delay, intellectual disability, and distinctive facial features. Affected individuals may also have skeletal abnormalities and require multidisciplinary care for symptom management.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(neurologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Intellectual disability
(neurologic)Speech delay
(neurologic)Motor coordination deficits
(neurologic)Autism spectrum features
(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
Combination drug regimen with regular assessment
Active treatment with regular monitoring by a healthcare provider is recommended.
Early Intervention Physical Therapy
Age-appropriate therapeutic exercises and developmental activities to promote motor skills, coordination, and functional mobility from an early age.
Developmental Psychology Support
Cognitive and behavioral assessments with tailored interventions to support learning, communication, and adaptive skills development.
Additional treatment options
Comprehensive Developmental Monitoring
Regular interdisciplinary assessments of growth, development, and emerging needs across all domains including motor, cognitive, and language.
monitoringTargeted Symptomatic Pharmacotherapy
Medication for specific associated symptoms such as attention difficulties, hyperactivity, or other neurological manifestations as clinically indicated.
medicationStructured Home Environment and Routine
Creation of consistent daily routines, structured learning environment, and supportive home setup to maximize developmental progress and independence.
lifestyleWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Kariminejad Neurodevelopmental Syndrome C5975371?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalMedication Comparisons
Compare medications used to treat Kariminejad Neurodevelopmental Syndrome C5975371. 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