Abstract

A 6-year-old girl presenting with a 6-month history of classical familial migraine, complicated by transitory hemiparesis and moyamoya disease diagnosed by MRI, is reported from the Kaiser Permanente Medical Center, Hayward, CA.

Highlights

  • Neuronal migration disorder as a cause of focal motor status epilepticus or epilepsia partialis continua in a child may not be excluded by the MRI and may require surgical intervention for diagnosis and treatment

  • MOYAMOYA DISEASE AND HEMIPLEGIC MIGRAINE A 6-year-old girl presenting with a 6-month history of classical familial migraine, complicated by transitory hemiparesis and moyamoya disease diagnosed by MRI, is reported from the Kaiser Permanente Medical Center, Hayward, CA

  • ADRENAL, ALACRIMAL, ACHALASIA SYNDROME The results of a British and European Paediatric Endocrinology Society, multicenter collaborative, questionnnaire study of the neurological complications of familial glucocorticoid deficiency syndrome are reported from the Hospital for Sick Children, Great Ormond Street, London

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Summary

Introduction

Neuronal migration disorder as a cause of focal motor status epilepticus or epilepsia partialis continua in a child may not be excluded by the MRI and may require surgical intervention for diagnosis and treatment. MOYAMOYA DISEASE AND HEMIPLEGIC MIGRAINE A 6-year-old girl presenting with a 6-month history of classical familial migraine, complicated by transitory hemiparesis and moyamoya disease diagnosed by MRI, is reported from the Kaiser Permanente Medical Center, Hayward, CA. Headaches occurred each week and were associated with nausea, vomiting, and photophobia.

Results
Conclusion
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