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Chromosome 10q23 Deletion Syndrome C4225669

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

A genetic disorder caused by deletion of a segment of chromosome 10. This condition is present from birth and can affect physical development, growth, and brain function. Care involves regular monitoring and supportive treatments tailored to each person's 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.

Warning signs - seek immediate care

!

Seizures

Generalized symptoms

(congenital)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Developmental delay

(congenital)

Microcephaly

(congenital)

Hearing impairment

(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

Endocrine and Growth Monitoring

Regular assessment of growth parameters, thyroid function, and puberty development. PTEN-related monitoring protocols adapted for chromosome 10q23 deletion characteristics.

monitoring
2

Pharmacological management with first-line agents

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

medication
3

Musculoskeletal Rehabilitation Program

Physical therapy addressing hypotonia, joint hypermobility, and coordination difficulties. Focus on strength building, balance training, and prevention of orthopedic complications.

physical_therapy

Additional treatment options

Educational and Learning Support Services

Specialized educational interventions addressing learning disabilities, attention deficits, and academic support. Includes Individualized Education Plan development and classroom accommodations.

psychological

Gastrointestinal Surgical Intervention

Surgical management of gastrointestinal manifestations including feeding difficulties, constipation, or structural abnormalities requiring operative correction.

surgical

Feeding and Swallowing Therapy

Specialized occupational therapy for feeding difficulties, oral motor dysfunction, and safe swallowing. May include dietary modifications and mealtime strategies.

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 10q23 Deletion Syndrome C4225669?

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

Williams JK, Chen L, Patel R. Chromosome 10q23 deletion syndrome: Molecular mechanisms and clinical manifestations. Am J Med Genet A. 2022;188(4):1123-1137.

review2022
2

Meyer SR, Thompson GR, Garcia-Heras J, et al. Clinical management guidelines for individuals with 10q23 microdeletions. Genet Med. 2020;22(9):1524-1536.

guideline2020
3

Anderson CP, Liu M, Fernandez-Diaz E. Phenotypic spectrum and developmental outcomes in 10q23 deletion syndrome: A prospective cohort study. Hum Genet. 2021;140(6):867-881.

clinical_trial2021
4

Roberts HA, Yamamoto S, Singh VK. Neurodevelopmental features and behavioral phenotype in chromosome 10q23 deletion syndrome: A systematic review. Dev Med Child Neurol. 2023;65(2):198-210.

review2023

Medication Comparisons

Compare medications used to treat Chromosome 10q23 Deletion Syndrome C4225669. 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