An unusual diagnosis for an usual test.
Andrea TrombettaVanessa MigliarinoFlavio FaletraEgidio BarbiGianluca TornesePublished 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.
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