SavedAdd your journal

Journals / Tıp Araştırmaları Dergisi / 2014 / Cilt: 12 - Sayı: 2

Isaacs’ Syndrome (Acquired Neuromyotonia): A Case Report

Isaac Sendromu (Edinsel Nöromyotoni): Olgu Sunumu

Gökhan KOYUNCU
İnci ÇEÇEN
Fatıma KARAKAYA
Zekiye TOKLU
Mehmet YAMAN
Pages
83–87
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Because of rarity of İsaac's disease, we are discussing the diagnosis.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Isaac's syndrome is charachterized by (potassium) channelopathy with muscle spasms and myokymia.
📊
Key Findings & Data:The patient came to our hospital because of muscle pains in arms and legs, weakness, concordance and muscle cramps which have continued for 20 days.
💡
Conclusion & Impact:Because of rarity of İsaac's disease, we are discussing the diagnosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Isaac's syndrome is charachterized by (potassium) channelopathy with muscle spasms and myokymia. İt is diagnosed in early adulthood. İt is mostly sporadic and underdiagnosed disorder. The patient came to our hospital because of muscle pains in arms and legs, weakness, concordance and muscle cramps which have continued for 20 days. The electromiyography of the patient shows myokymias. Because of rarity of İsaac's disease, we are discussing the diagnosis.

Özet

Isaacs' sendromu kas krampları ve miyokimilerle karakterize bir (Potasyum) kanolapatisidir. Genellikle genç erişkinlerde, seyrek görülen, çoğunlukla sporadik bir hastalıktır. Hastanemize 20 gündür devam etmekte olan kol ve bacaklarda kas ağrısı, güçsüzlük, uyuşma ve kas krampları nedeniyle başvuran hastanın elektromiyografisinde (EMG) görülen miyokimiler ile isaacs' sendromu tanısı koyduğumuz olguyu nadir görülmesi nedeniyle tartıştık.

🔖

Cite This Article

KOYUNCU, G., ÇEÇEN, İ., KARAKAYA, F., TOKLU, Z., YAMAN, M. (2014). Isaacs’ Syndrome (Acquired Neuromyotonia): A Case Report. Tıp Araştırmaları Dergisi, Cilt: 12 - Sayı: 2, 83–87. https://ajindex.com/articles/361799

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (5)

  1. Sukaj intanakarn D, Mitrabhakdi E, Phanthumchinda K. Acquired Neuromyotonia (isaacs syndrome): Case Report with Autonomic Physiologic Studies. Med Assoc Thai 2006; 89(8): 1308-1312.
  2. Gürğöze MK, Poyrazoğlu MH, Mirza ve ark. Mezenğioproliferatif ğlomerulonefrit ile birlikte olan bir Isaacs sendromu vakası. Çocuk Sağlığı ve Hastalıkları Dergisi 2006; 49: 312-314.
  3. Roland Dominic G. Jamora, T. Umapathi, Louis C.S. Tan. Case report Finger flexion resembling focal dystonia in Isaacs’ syndrome. Parkinsonism and Related Disorders 2006; 12: 61-63. Dhand UK. Isaacs syndrome: clinical and electrophys1olog1cal response to gabapentin. Muscle Nerve 2006; 34: 646-650. Isaacs H. syndrome of continuous muscle fiber activity. Neurol Neurosurg Psychiatry 1961; 24: 319-325.
  4. Tanosaki M, Baba M, Miura H, Matsunaga M, Arimura K. Reversible F-Wave hyperexcitability associated With antibodies to potassium channels in Isaacs syndrome. Eur Neurol 1999; 6: 95-98.
  5. Pan H-L, Eisenach JC, Chen S-R. Gabapentin suppresses ectopic nevre discharges and reverses allodynia in neuropathic rats. Pharmacol Exp Ther 1999; 288: 1026-1030.