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Updated: Feb 24, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

モルバン症候群のまれな青年期発症：診断の課題と治療反応

Muhammad Umar¹, Majeed Ullah², Umm E Salma Shabbar Banatwala³

¹Khairpur Medical College Khairpur Pakistan.

Clinical case reports

|February 23, 2026

Abstract:

Morvan syndrome is a rare autoimmune disorder that predominantly affects adults, but it can also present in adolescents with atypical symptoms. This case of a 17-year-old patient exhibited severe back pain, muscle twitching, visual hallucinations, and hyponatremia, without the thymoma or malignancy commonly observed in adult cases. Early diagnosis and prompt immunotherapy with corticosteroids and plasmapheresis resulted in significant symptom improvement, highlighting the importance of timely intervention in complex neuroimmunological disorders.

キーワード:

モルバン症候群自己免疫性脳症自己免疫性神経疾患免疫療法反応

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