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SCAPULOPERONEAL PHENOTYPES IN THREE GENETICALLY DISTINCT PATIENTS: DIAGNOSTIC AND ELECTROPHYSIOLOGICAL IMPLICATIONS

Nur TURKMEN, Ozlem Ergin BETON, Sule BILEN, Yigit Emre DAGDELEN

Neurological Sciences and Neurophysiology - 2025;42(4):194-196

Ankara Bilkent City Hospital, Ankara, Türkiye

 

Scapuloperoneal syndrome (SPS) refers to a clinical phenotype, characterized by weakness in the scapular and peroneal muscles, often presenting with scapular winging and foot drop. This constellation of symptoms may arise from either myopathic or neurogenic origins and can be associated with a wide array of genetic disorders. We present three genetically distinct patients exhibiting the SPS phenotype to highlight the clinical, electrophysiologic, and molecular heterogeneity of this presentation.