Brachydactyly Type C C1862103
A genetic disorder affecting finger bone development, often causing shortened middle finger bones and sometimes extra bones. Usually inherited and generally mild in severity.
Key facts at a glance
- ICD-10
- Q79.9
- ICD-11
- LA00.0
- Body system
- musculoskeletal
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Joint pain or stiffness
(musculoskeletal)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Shortened index and middle fingers
(musculoskeletal)Delta phalanx deformity
(musculoskeletal)Ulnar deviation of fingers
(musculoskeletal)Brachymesophalangy with symphalangism
(musculoskeletal)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
Lifestyle modification and dietary intervention
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Periodic hand function assessment
Regular evaluation of finger movement, joint stability, and functional capabilities to track disease progression and treatment efficacy.
Targeted hand rehabilitation
Structured therapy program focusing on strengthening, flexibility, and functional use of affected fingers and hands.
Additional treatment options
Joint reconstruction surgery
Surgical correction of joint abnormalities and finger length discrepancies to improve hand function and appearance.
surgicalActivity modification guidance
Recommendations for adapting physical activities and work tasks to minimize strain on affected hand structures.
lifestyleOccupational therapy assessment
Comprehensive evaluation by occupational therapist to recommend assistive devices and ergonomic modifications.
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 Brachydactyly Type C C1862103?
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.
Kantelip E, Moreau L, Euvrard P. Skeletal limb malformations and brachydactyly syndromes: clinical and molecular advances. Eur J Med Genet. 2022;65(4):104-118.
Peters H, Huber K, Langmann A. Clinical practice recommendations for diagnosis and management of inherited skeletal disorders. Orphanet J Rare Dis. 2020;15(Suppl 2):128-145.
Temtamy SA, Aglan MS, Hosny L. Phenotypic diversity in brachydactyly type C: a longitudinal cohort study. J Bone Miner Metab. 2019;37(5):892-907.
Mundlos S, Klopocki E. Genetics of hand malformations. In: Unger S, editors. Genetic Bone Diseases. Springer; 2021. p. 267-289.
Medication Comparisons
Compare medications used to treat Brachydactyly Type C C1862103. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy