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Bardet Biedl Syndrome 3 C1859564

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

One of several genetic subtypes of a rare disorder affecting cellular cilia function. Leads to progressive vision loss, obesity, kidney problems, and possible developmental challenges. Coordinated specialist care is essential.

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

Rod-cone dystrophy

(congenital)

Postaxial polydactyly

(congenital)

Renal malformation

(genitourinary)

Hypogonadotropic hypogonadism

(endocrine)

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

Lifestyle modification and dietary intervention

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Ophthalmologic surveillance

Regular retinal examinations and visual field testing to monitor progressive cone-rod dystrophy typical of BBS3 variant.

monitoring
3

Environmental and safety modifications

Home and environmental adaptations including lighting improvements, contrast enhancement, and safety measures to prevent accidents.

lifestyle

Additional treatment options

Obesity prevention and management

Calorie-controlled diet with emphasis on satiety-promoting foods and avoidance of high-glycemic foods to manage weight.

dietary

Urogenital anomaly correction

Surgical repair of structural urogenital abnormalities when present, typically addressed in early childhood.

surgical

Academic and vocational support

Educational accommodations, learning support services, and career counseling to maximize academic and professional potential.

psychological

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 3 C1859564?

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 3 C1859564. 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