This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Classification

Authoring team

Congenital syndactyly may be classified according to the:

  • isolated anomaly or syndromic association
  • tissues fused:
    • simple - soft tissue alone from the proximal end of the digit
    • complex - bone synostosis (metacarpal or phalangeal) and soft tissue
    • acrosyndactyly - complex syndactyly characterised by fusion of the bones distally but not proximally; fenestrations are usually present between the bones proximally and associated with constriction ring syndrome
  • extent of fusion proximal-to-distal:
    • complete - fusion from web space to distal interphalangeal joints; can be associated with synonychia which is a shared or common fingernail
    • incomplete
  • number of digits affected eg single versus multiple
  • unilateral or bilateral
  • site affected:
    • hand
    • foot
    • both

Reference

  1. Buck-Gramcko D. Congenital malformations of the hand and forearm. Chir Main. 2002 Mar;21(2):70-101

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.