A Case of Lafora Disease Diagnosed by Axillary Skin Biopsy

• मुख्य लेखकों: Elife KIMILOĞLU (लेखक), Pelin AKBAŞ (लेखक), Özgül ESEN ÖRE (लेखक), Çağla TURAN (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Federation of Turkish Pathology Societies, 2021-09-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...