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A registry of achondroplasia: a 6-year experience from the Czechia and Slovak Republic.

Martin PeslHana VerescakovaLinda SkutkovaJana StrenkovaPavel Krejci
Published in: Orphanet journal of rare diseases (2022)
The registry collected the clinical information of 51 pediatric ACH patients during its 6 years of existence, corresponding to ~ 60% of ACH patients living in the Czechia and Slovak Republic. The registry continues to collect ACH patient data with annual frequency to monitor the growth and other parameters in preparation for future therapy.
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