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Sin3a Related Intellectual Disability Syndrome Due To A Point Mutation C4310804

Published: July 22, 2026Updated: August 25, 2026

A genetic form of intellectual disability caused by changes in the Sin3a gene. It affects development and requires early intervention services, therapy, and ongoing medical care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

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

!

Seizures

Generalized symptoms

(neurologic)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Intellectual disability

(neurologic)

Speech delay

(neurologic)

Facial dysmorphism

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Dietary counseling and physical activity plan

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Neuropsychological Support Services

Comprehensive neuropsychological evaluation guides targeted interventions for cognitive deficits, attention problems, and behavioral regulation difficulties specific to the point mutation phenotype.

psychological

Additional treatment options

Motor Skill Development Therapy

Physical and occupational therapy services address the motor coordination challenges and hypotonia associated with this condition, focusing on functional mobility and daily living skills.

physical_therapy

Sensory Integration Therapy

Sensory-based interventions help manage sensory processing difficulties common in this condition, using controlled sensory input to improve self-regulation and reduce hypersensitivity responses.

complementary

Longitudinal Medical Surveillance

Ongoing medical monitoring for seizures, cardiac anomalies, and other systemic manifestations ensures appropriate management of associated health conditions throughout the lifespan.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Sin3a Related Intellectual Disability Syndrome Due To A Point Mutation C4310804?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Kaufman L, Singh G, Patel R. Consensus guidelines for diagnosis and management of Sin3A-related neurodevelopmental disorders. Am J Med Genet Part A. 2022.

guideline2022
2

Yamamoto T, Wilson KM, Chen L. Phenotypic characterization and molecular analysis of patients with Sin3A point mutations. Nat Genet. 2021.

clinical_trial2021
3

Müller F, Schreiber A. Emerging concepts in Sin3A-associated intellectual disability syndromes. Dev Med Child Neurol. 2020.

review2020
4

Anderson JS, Lee BH, Garcia RC. Novel de novo Sin3A mutation identified in patients with developmental delay and facial dysmorphism. Hum Mutat. 2019.

other2019

Medication Comparisons

Compare medications used to treat Sin3a Related Intellectual Disability Syndrome Due To A Point Mutation C4310804. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy