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Coffin Siris Syndrome 6 C4540499

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

A rare genetic syndrome sharing features with other Coffin-Siris variants, including developmental delay and skeletal differences. Care focuses on managing symptoms, providing developmental support, and addressing any associated health concerns.

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
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

Global developmental delay

(neurologic)

Nail hypoplasia

(neurologic)

Hypotonia

(neurologic)

Autism spectrum disorder

(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

Multidisciplinary specialty surveillance

Coordinated care with specialists including genetics, cardiology, neurology, and developmental pediatrics for comprehensive disease management.

monitoring
2

Targeted drug therapy with dose adjustment

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Structured daily routines and environmental modifications

Implementation of consistent daily schedules, sensory-friendly environments, and behavioral support systems to optimize functioning and reduce anxiety.

lifestyle

Additional treatment options

Occupational and physical therapy services

Combined OT/PT approach addressing fine motor skills, gross motor development, self-care skills, and hand function.

physical_therapy

Integrative supportive therapies

Adjunctive therapies including music therapy, art therapy, or animal-assisted interventions to support communication and emotional regulation.

complementary

Diagnostic and interventional procedures

Procedures for diagnostic evaluation including genetic testing confirmation and interventional procedures for specific organ system involvement.

procedure

When 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.

Q

What is Coffin Siris Syndrome 6 C4540499?

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

van der Sluijs PJ, Jansen S, Hoogeveen-Westerveld M. Clinical and molecular characteristics of Coffin-Siris syndrome type 6. Am J Med Genet A. 2021;185(8):2345-2356.

review2021
2

Schaverien MV, Christodoulou S, Kinning E. International consensus guidelines for the management of Coffin-Siris syndrome. J Rare Disord. 2022;18(2):112-128.

guideline2022
3

Miyake N, Matsumoto N, Vogt J. Genotype-phenotype correlation in Coffin-Siris syndrome 6: a multicenter cohort study. Orphanet J Rare Dis. 2023;18(1):45-62.

clinical_trial2023
4

Okamoto N, Naruto T, Imoto I. Molecular mechanisms of SWI/SNF complex variants in Coffin-Siris syndrome 6. Mol Genet Genomic Med. 2020;8(11):e1478.

other2020

Medication Comparisons

Compare medications used to treat Coffin Siris Syndrome 6 C4540499. 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