Login / Signup

An unusual diagnosis for an usual test.

Andrea TrombettaVanessa MigliarinoFlavio FaletraEgidio BarbiGianluca Tornese
Published in: Italian journal of pediatrics (2020)
HMO is a genetic condition whose diagnosis can be challenging, especially in females. Every pediatricians should consider a skeletal dysplasia in case of unexplained growth delay and a skeletal survey might be fundamental in reaching a diagnosis.
Keyphrases
  • cross sectional
  • copy number