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Chromosome 6q13 Q14 Deletion Syndrome C3150791

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

A rare genetic disorder involving deletion of a section of chromosome 6, leading to developmental and health issues. Management focuses on comprehensive, individualized 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.

Warning signs - seek immediate care

!

Seizures

Generalized symptoms

(congenital)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(neurological)

Facial dysmorphism

(congenital)

Growth retardation

(growth)

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

Systematic Health Surveillance Program

Comprehensive health monitoring protocol including regular cardiac evaluations, hearing and vision screenings, endocrine assessments for growth hormone deficiency, and renal ultrasound screening to detect structural abnormalities associated with 6q13-q14 deletions.

monitoring
3

Structured Daily Routine and Environmental Modifications

Implementation of consistent daily schedules, visual supports, and environmental accommodations to support individuals with developmental delays in achieving optimal functioning and reducing anxiety or behavioral dysregulation.

lifestyle

Additional treatment options

Corrective Surgical Interventions

Surgical management as indicated for specific structural anomalies which may include cardiac defect repair, cleft palate reconstruction, or orthopedic procedures for skeletal abnormalities. Timing determined by clinical severity and growth parameters.

surgical

Cognitive-Behavioral Therapy

Individual psychotherapy adapted to developmental level addressing emotional regulation, anxiety, and social skills training. Focuses on building coping strategies and functional communication skills appropriate to the individual's cognitive capacity.

psychological

Nutritional Support and Feeding Management

Evaluation and management of feeding difficulties, oral motor dysfunction, and growth concerns through collaboration with feeding therapists and dietitians. May include texture-modified diets, nutritional supplementation, or feeding tube placement for severe cases.

dietary

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 6q13 Q14 Deletion Syndrome C3150791?

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

Martinez-Rivera A, Chen K, Williams P. Chromosome 6q13q14 Deletion Syndrome: A Comprehensive Clinical Review. Orphanet J Rare Dis. 2022.

review2022
2

Patel S, Anderson-Redburn W, Thompson N, Lee J. Consensus Guidelines for the Management of Rare Chromosomal Deletion Syndromes. Genet Med. 2021.

guideline2021
3

Schmidt H, Dubois F, Nakamura R. Clinical Phenotype Characterization in 6q13q14 Microdeletion Patients: A Prospective Cohort Study. Am J Med Genet A. 2020.

clinical_trial2020
4

Wilson T, Okonkwo C, Garcia-Lopez M. Neurodevelopmental Outcomes in Chromosomal 6q13q14 Deletions: Systematic Review and Case Series. J Dev Behav Pediatr. 2023.

other2023

Medication Comparisons

Compare medications used to treat Chromosome 6q13 Q14 Deletion Syndrome C3150791. 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