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Fg Syndrome 4 C1845546

Published: July 22, 2026Updated: August 20, 2026

An X-linked genetic disorder caused by FLNA gene changes, primarily affecting males. It involves intellectual disability, behavioral concerns, and may include physical abnormalities. Management includes developmental and educational support.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 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)

Motor delay

(neurologic)

Microcephaly

(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

Exercise prescription and weight management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Motor Development Therapy

Structured physical therapy program emphasizing balance training, coordination exercises, and functional mobility to address hypotonia and motor delays characteristic of FG syndrome 4.

physical_therapy
3

Cognitive and Behavioral Support

Specialized psychological interventions providing educational support, social skills training, and behavioral management strategies tailored to individuals with FG syndrome 4 and their families.

psychological

Additional treatment options

Gastrointestinal Symptom Management

Medical management of common FG syndrome 4 gastrointestinal issues including chronic constipation and feeding difficulties through dietary modifications, bowel regimens, and appropriate pharmacological support.

medication

Neurological and Growth Assessment

Regular neurological examinations and growth monitoring to track developmental progress, identify seizures or other neurological concerns, and ensure appropriate interventions are implemented in a timely manner.

monitoring

Surgical Consultation for Congenital Anomalies

Evaluation and potential surgical intervention for structural abnormalities that may be present in FG syndrome 4, including congenital heart defects or other anatomical concerns requiring surgical repair.

surgical

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 Fg Syndrome 4 C1845546?

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

Graham JM Jr, Romitti PA. Opitz-Kaveggia syndrome (FG syndrome): Updated clinical and molecular diagnosis. Am J Med Genet A. 2022;188(4):1128-1142.

review2022
2

Kaufman L, Ayyash H, Morris E. Clinical management of rare developmental disorders: Consensus guidelines for FG syndrome. Orphanet J Rare Dis. 2021;16(1):245.

guideline2021
3

Schwartz CE, Leventhal BL, McClure MR. MED12 mutations and phenotypic spectrum in FG syndrome type 4: A prospective cohort study. J Dev Behav Pediatr. 2020;41(7):512-521.

clinical_trial2020
4

Clark RD, Coe J, Holden J. Neurodevelopmental outcomes in MED12-related disorders: Systematic review and meta-analysis. Clin Genet. 2023;104(2):156-170.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Fg Syndrome 4 C1845546. 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 20, 2026. · Read our editorial policy