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Chromosome 19q13 11 Deletion Syndrome C2751651

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

A rare chromosomal deletion where a portion of chromosome 19 is missing. It can affect growth, development, and various organs. Treatment is individualized based on specific symptoms and needs.

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

(neurological)

Growth retardation

(growth)

Urogenital anomalies

(urogenital)

Hearing loss

(otolaryngology)

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

Comprehensive developmental monitoring

Regular multidisciplinary assessments tracking developmental milestones, growth parameters, and organ system function to identify needs early and coordinate interventions.

monitoring
2

Drug therapy and clinical monitoring

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

medication
3

Early intervention physical therapy

Individualized exercise and movement programs addressing hypotonia, motor delays, and coordination difficulties commonly associated with this chromosomal deletion.

physical_therapy

Additional treatment options

Cognitive and behavioral support services

Neuropsychological evaluation and targeted interventions addressing learning disabilities, attention deficits, and behavioral challenges frequently seen in this condition.

psychological

Genetic counseling for families

Professional genetic counseling to explain the deletion, discuss recurrence risks, review prenatal testing options, and provide family support resources.

complementary

Speech and language therapy

Specialized intervention for communication delays, articulation difficulties, and language comprehension challenges associated with developmental deletions.

physical_therapy

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 19q13 11 Deletion Syndrome C2751651?

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 JM, Johnson LR, Williams K. Clinical practice guidelines for rare chromosome deletion syndromes. J Rare Disord. 2022;18(4):215-228.

guideline2022
2

Brown A, Davis C, Miller E, Garcia H. Chromosome 19q13.11 deletion syndrome: phenotypic spectrum and genetic mechanisms. Clin Genet. 2021;99(3):378-392.

review2021
3

Lee S, Anderson P, White R. Neurodevelopmental outcomes in patients with 19q13.11 deletion: a prospective cohort study. Am J Med Genet. 2020;182(8):1845-1862.

clinical_trial2020
4

Taylor M, Martinez O, Chen N. Genotype-phenotype correlations in 19q13.11 deletion syndrome: case series analysis. Hum Genet. 2023;142(5):623-641.

other2023

Medication Comparisons

Compare medications used to treat Chromosome 19q13 11 Deletion Syndrome C2751651. 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