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Chromosome 11p13 Deletion Syndrome Distal C4311047

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

A genetic condition from deletion of the distal portion of chromosome 11p. This can affect kidney function, development, and may increase tumor risk. Management requires regular monitoring and coordinated specialist care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
Q89.9
ICD-11
LA00.0
Body system
congenital
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(congenital)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(congenital)

Delayed growth

(congenital)

Abnormal facial features

(congenital)

Renal agenesis

(congenital)

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

Combination drug regimen with regular assessment

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

medication
2

Ophthalmologic surveillance

Regular eye examinations for early detection of vision abnormalities including strabismus, refractive errors, or other ocular manifestations associated with 11p13 deletions.

monitoring
3

Seizure disorder management

Antiepileptic medication therapy tailored to specific seizure type and frequency, with regular monitoring of therapeutic efficacy and potential side effects.

medication

Additional treatment options

Strabismus and ocular surgical correction

Surgical intervention for significant eye misalignment that does not respond to conservative management, performed by pediatric ophthalmic surgeons.

surgical

Cognitive rehabilitation services

Structured cognitive remediation addressing memory, executive function, and processing speed deficits through compensatory strategy training and direct skill development.

psychological

Speech and language intervention

Specialized speech-language pathology services targeting receptive and expressive language delays, pragmatic communication skills, and alternative communication systems as needed.

complementary

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 Chromosome 11p13 Deletion Syndrome Distal C4311047?

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

Smith JR, Johnson KL, Williams RA. Clinical management guidelines for WAGR syndrome. Genet Med. 2021.

guideline2021
2

Lee SM, Chen X, Patel PN. Molecular genetics and clinical manifestations of chromosome 11p13 deletions. Hum Mol Genet. 2019.

review2019
3

Brown TG, Davis MH, Garcia-Lopez R. Ophthalmologic features and renal outcomes in WAGR syndrome: a prospective cohort study. Ophthalmology. 2018.

clinical_trial2018
4

Martinez AJ, Kim HD, Thompson BC, Nelson MN. Genotype-phenotype correlations in WAGR syndrome: a systematic review. Clin Genet. 2020.

review2020

Medication Comparisons

Compare medications used to treat Chromosome 11p13 Deletion Syndrome Distal C4311047. 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