A Case of Lafora Disease Diagnosed by Axillary Skin Biopsy

• Κύριοι συγγραφείς: Elife KIMILOĞLU (Συγγραφέας), Pelin AKBAŞ (Συγγραφέας), Özgül ESEN ÖRE (Συγγραφέας), Çağla TURAN (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Federation of Turkish Pathology Societies, 2021-09-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

Lafora disease is a severe form of progressive myoclonic epilepsy with autosomal recessive inheritance diagnosed by inclusion body in biopsy. A 26-year-old woman was admitted due to complaints of frequent twitches and fainting. The 0.5x0.3x0.3 cm axillary skin punch biopsy was subjected to routine h...