Clinodactyly is a congenital angular deformity of the middle phalanx in the radioulnar plane that is usually bilateral and involves the small finger, although other digits also can be affected.1 Clinodactyly is an autosomal dominant condition, and it occurs either in isolation or in association with other syndromes.2 Unless clinodactyly is severe, it typically causes little-to-no functional impairment, especially if the little finger is involved. For this reason, observation alone is usually sufficient, and surgical intervention is reserved only for cases in which the deformity interferes with function or for cosmetic purposes. Surgical options for clinodactyly include closing, opening and reverse wedge osteotomies and physiolysis; treatment decisions should be based on the underlying pathology, age of the patient, as well as other factors. 1,3
Pathophysiology
Related Anatomy
Exam Findings, Signs and Positive Tests
Work-Up Options
Incidence and Related Conditions
Differential Diagnosis
Reproduced from the International statistical classification of diseases and related health problems, 10th revision, Fifth edition, 2016. Geneva, World Health Organization, 2016 https://apps.who.int/iris/handle/10665/246208
The typical patient is a 9-year-old, right-or left-handed boy with Down’s syndrome. His parents noticed a minor deformity of his left little finger years earlier, as the digit was abnormally bent and deviated slightly towards the fourth finger. As the boy grew, the angulation of the deformity became larger and more noticeable. Consequently, his parents took him to a physician for a clinical evaluation. The physician diagnosed the boy with clinodactyly based on his physical examination and patient history. Noting that the condition did not significantly impair his hand function, the physician recommended ongoing observation of the finger until or unless the boy developed severe functional limitations. 1-4
Surgical Complications:
Cited
New Articles
Review
Classics