Kanmaz, SedaŞimşek, ErdemSerin, Hepsen MineErdoğan, Murat KadriYılmaz, SanemAktan, GülGökben, Sarenur2021-05-032021-05-0320192147-94452587-2478https://doi.org/10.4274/jpr.galenos.2018.60590https://app.trdizin.gov.tr/makale/TXpZd05qQXpNdz09https://hdl.handle.net/11454/71709Hereditary neuropathy with a liability to pressure palsies (HNPP) represented by recurrent focal pressure neuropathies is rare in childhood. Here we present a 10-year-old girl admitted to our hospital with a recurrent weakness in her foot and diagnosed as HNPP with a quick Multiplex Ligation-dependent Probe Amplification test revealing PMP22 deletion.en10.4274/jpr.galenos.2018.60590info:eu-repo/semantics/openAccess[No Keywords]Article62163165