Optimising the diagnosis and referral of achondroplasia in Europe: European Achondroplasia Forum best practice recommendations.
Valerie Cormier-DaireMoeenaldeen AlSayedInês AlvesJoana BengoaTawfeg Ben-OmranSilvio BoeroSvein FredwallCatherine GarelEncarna Guillen-NavarroMelita IrvingChristian LampeMohamad MaghnieGeert MortierSérgio B SousaKlaus MohnikePublished in: Orphanet journal of rare diseases (2022)
The European Achondroplasia Forum guiding principles of management recommend diagnosis of achondroplasia as early as possible. If concerns are raised at routine ultrasound, second line investigation should be implemented so that the diagnosis can be reached as soon as possible for ongoing management. Clinical and radiological examination supported by molecular testing is the most effective way to confirm diagnosis of achondroplasia after birth. Referral to a centre specialised in achondroplasia care should be made as soon as possible on suspicion or confirmation of diagnosis. In countries or regions where there are no official skeletal dysplasia reference or specialist centres, priority should be given to their creation or recognition, together with incentives to improve the structure of the existing multidisciplinary team managing achondroplasia. The length of delay between diagnosis of achondroplasia and referral to a specialist centre warrants further research.