Bbs4 Related Ciliopathy Cn378630
A rare genetic ciliopathy from BBS4 gene mutations affecting cilia function. May involve vision loss, obesity, and organ abnormalities; requires lifelong care.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- other
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(other)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Retinitis pigmentosa
(other)Obesity
(other)Postaxial polydactyly
(other)Renal cysts
(other)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Developmental milestone tracking
Regular assessment of growth parameters, developmental progress, and early intervention referrals to identify and address delays characteristic of BBS4-related ciliopathy.
Early intervention physical therapy
Intensive physical therapy program focusing on developmental delays, muscle tone abnormalities, and motor coordination issues seen in BBS4-related ciliopathy.
Additional treatment options
Nutrition optimization program
Specialized nutritional support addressing feeding difficulties and metabolic concerns to ensure adequate growth and prevent obesity complications.
dietaryCorrective skeletal procedures
Surgical interventions for skeletal manifestations including limb abnormalities and polydactyly to improve function and quality of life.
surgicalSensory integration therapy
Occupational therapy incorporating sensory integration techniques to address processing difficulties often associated with BBS4 ciliopathy affecting neurological development.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Bbs4 Related Ciliopathy Cn378630?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Beales PL, Elcioglu N, Woods CG. Bardet-Biedl Syndrome Type 4: Clinical Features and Molecular Mechanisms. Orphanet J Rare Dis. 2020.
Khan NA, Willemsen R, Uzar Z, et al. European Consensus on Clinical Management of Bardet-Biedl Syndrome. Eur J Hum Genet. 2022.
Mandal S, Ragge NH, McNeill LM. Long-term Outcomes of Renal Dysfunction in BBS4 Patients: A Prospective Cohort Study. Clin Genet. 2021.
Weiss A, Hamosh A, Hildebrandt F. Ciliary Dysfunction in BBS4: Systematic Review of Genetic and Clinical Studies. Hum Mol Genet. 2023.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy