Skip to content

Bardet Biedl Syndrome 2 C2936863

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

A genetic disorder affecting multiple body systems due to ciliary dysfunction. Features include vision loss, obesity, polydactyly, kidney disease, and developmental delays. Treatment focuses on symptom management and regular monitoring.

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.

Warning signs - seek immediate care

!

Rod-cone dystrophy (retinal degeneration)

Generalized symptoms

(congenital)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Obesity

(endocrine)

Postaxial polydactyly

(musculoskeletal)

Hepatic fibrosis

(hepatobiliary)

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 comprehensive monitoring

Regular multidisciplinary surveillance including ophthalmologic exams, renal function tests, metabolic screening, and developmental assessments to detect and manage complications early.

monitoring
2

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
3

Obesity management program

Structured caloric restriction combined with regular physical activity adapted to visual and motor abilities to prevent secondary complications including diabetes and cardiovascular disease.

lifestyle

Additional treatment options

Vision rehabilitation services

Orientation and mobility training, low-vision aids, and adaptive technologies to maximize functional independence despite progressive retinal degeneration.

lifestyle

Psychological support and counseling

Individual and family counseling to address learning difficulties, social challenges, and coping with progressive vision loss associated with the condition.

psychological

Polydactyly correction

Surgical removal of extra digits when functionally limiting or for cosmetic purposes, typically performed in early childhood.

surgical

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 2 C2936863?

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 2 C2936863. 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