Hereditary Neuropathy with Liability to Pressure Palsy: A Case Diagnosed with a Quick Multiplex Ligation-dependent Probe Amplification Test

Kanmaz, SedaŞimşek, ErdemSerin, Hepsen MineErdoğan, Murat KadriYılmaz, SanemAktan, GülGökben, Sarenur2020-12-012020-12-0120192147-94452587-2478https://doi.org/10.4274/jpr.galenos.2018.60590https://app.trdizin.gov.tr//makale/TXpZd05qQXpNdz09https://hdl.handle.net/11454/67061Hereditary 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/openAccess0-BelirlenecekHereditary Neuropathy with Liability to Pressure Palsy: A Case Diagnosed with a Quick Multiplex Ligation-dependent Probe Amplification TestArticle62163165N/A