Please confirm topic selection

Are you sure you want to trigger topic in your Anconeus AI algorithm?

Please confirm action

You are done for today with this topic.

Would you like to start learning session with this topic items scheduled for future?

Updated: Mar 11 2024

Radial Clubhand (radial deficiency)

Images
https://upload.orthobullets.com/topic/6067/images/TAR - xray - colorado_moved.jpg
https://upload.orthobullets.com/topic/6067/images/Case A - xray - Kosin_moved.jpg
https://upload.orthobullets.com/topic/6067/images/clinical photo - colorado_moved.jpg
https://upload.orthobullets.com/topic/6067/images/classification def.jpg
https://upload.orthobullets.com/topic/6067/images/Case A - clinical photo - Kosin_moved.jpg
https://upload.orthobullets.com/topic/6067/images/xray - colorado_moved.jpg
  • Summary
    • Radial Clubhand is a rare birth defect characterized by a deformity of hand, with perpendicular relationship between forearm and wrist, and an absent thumb. 
    • Diagnosis is made on physical exam.
    • Treatment may be observation or surgical reconstruction when the child is around 6 months of age. 
  • EPIDEMIOLOGY
    • Incidence
      • rare
        • 1 per 100,000
      • anatomic location
        • bilateral in 50-72%
        • thumb usually deficient as well
  • Etiology
    • Genetics
      • likely related to sonic hedgehog gene
      • most commonly result from spontaneous mutations
    • Associated with
      • TAR
        • autosomal recessive condition with thrombocytopenia and absent radius
        • different in that thumb is typically present
      • Fanconi's anemia
        • autosomal recessive condition with aplastic anemia
        • Fanconi screen and chromosomal breakage test to screen
        • treatment is bone marrow transplant
      • Holt-Oram syndrome
        • autosomal dominant condition characterized by cardiac defects
      • VACTERL Syndrome
        • vertebral anomalies, anal atresia, cardiac abnormalities, tracheoesophageal fistula, renal agenesis, and limb defects)
      • VATER Syndrome
        • vertebral anomalies, anal atresia, tracheoesophageal fistula, esophageal atresia, renal agenesis)
  • Classification
      • Bayne and Klug Classification
      • Type I
      • Deficient distal radial epiphysis
      • Type II
      • Deficient distal and proximal radial epiphyses
      • Type III
      • Present proximally (partial aplasia)
      • Type IV
      • Completely absent (total aplasia - most common)
  • Presentation
    • Physical exam
      • deformity of hand with perpendicular relationship between forearm and wrist
      • absent thumb
      • perform careful elbow examination
  • Imaging
    • Radiographs
      • entire radius and often thumb is absent
    • Laboratory
      • must order CBC, renal ultrasound, and echocardiogram to screen for associated conditions
  • Treatment
    • Nonoperative
      • passive stretching
        • target tight radial-sided structures
      • observation
        • indicated if absent elbow motion or biceps deficiency
          • hand deformity allows for extra reach to mouth in presence of a stiff elbow
    • Operative
      • hand centralization
        • indications
          • good elbow motion and biceps function intact
          • done at 6-12 months of age
          • followed by tendon transfers
        • contraindications
          • older patient with good function
          • patients with elbow extension contracture who rely on radial deviation
          • proximate terminal condition
        • technique
          • involves resection of varying amount of carpus, shortening of ECU, and, if needed, an angular osteotomy of the ulna (be sure to spare ulnar distal physis)
          • may do as two stage procedure in combination with a distraction external fixator
          • if thumb deformity then combine with thumb reconstruction at 18 months of age
Card
1 of 5
Question
1 of 10
Private Note

Attach Treatment Poll
Treatment poll is required to gain more useful feedback from members.
Please enter Question Text
Please enter at least 2 unique options
Please enter at least 2 unique options
Please enter at least 2 unique options