Skip to content

Bardet Biedl Syndrome 5 C3892039

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

A rare inherited syndrome affecting multiple organ systems through ciliary defects. Presents with vision impairment, weight gain, extra digits, and kidney issues. Multidisciplinary approach helps address complex 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
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(congenital)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Learning disability

(neurological)

Postaxial polydactyly

(congenital)

Diabetes mellitus

(endocrine)

Hearing loss

(ent)

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

Annual renal function assessment

Regular monitoring of kidney structure and function through imaging and laboratory tests to detect abnormalities early.

monitoring
2

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
3

Postaxial polydactyly removal

Surgical excision of extra digits on hands and feet, typically performed within the first year of life to optimize functional outcomes.

surgical

Additional treatment options

Vision rehabilitation services

Low vision aids, orientation and mobility training, and adaptive techniques to maximize functional vision and independence.

lifestyle

Motor skill development program

Physical therapy to improve coordination, strength, and gross motor skills affected by the syndrome.

physical_therapy

Genetic counseling for family

Comprehensive genetic counseling to explain inheritance patterns, recurrence risks, and available family planning options.

complementary

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 Bardet Biedl Syndrome 5 C3892039?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Bardet Biedl Syndrome 5 C3892039. 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