Dyke –Davidoff – Masson Syndrome in a 28 years old pregnant woman – A rare case report

Authors

  • Ashmita Yadav Department of Neurosurgery, Nobel Medical College Teaching Hospital, Biratnagar
  • Pramod Kumar Chaudhary Department Neurosurgery, Nobel Medical College and Teaching Hospital Biratnagar, Koshi, Nepal
  • Prakash Kafle Department of Neurosurgery, Nobel Medical College Teaching Hospital, Biratnagar
  • Edmond Jonathan Department of Neurosurgery, Nobel Medical College Teaching Hospital, Biratnagar, Koshi, Nepal
  • Sabin Jung Shah Department of Neurosurgery, Nobel Medical College Teaching Hospital,Biratnagar, Koshi, Nepal

DOI:

https://doi.org/10.3126/egn.v5i01.68451

Keywords:

Antiepileptic, DDM, Hemi atrophy, Seizure

Abstract

Dyke -Davidoff- Masson (DDM) Syndrome is rare neurological disorder commonly affecting the children but is rarely reported in adults as well. It mostly presents with seizure, hemiparesis followed by mental retardation and facial asymmetry. We here in report a case of 28 years old female (G3P2A0) with 34+ weeks of pregnancy who presented with generalized tonic clonic seizures and was incidentally diagnosed as DDM. She was managed with an External ventricular drain and antiepileptic medication. This case report aims to draw the attention of health care professionals to keep DDM as a differential in a patient with seizure. 

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Published

2024-08-06

How to Cite

Yadav , A., Kumar Chaudhary , P., Kafle, P., Jonathan , E., & Jung Shah, S. (2024). Dyke –Davidoff – Masson Syndrome in a 28 years old pregnant woman – A rare case report. Eastern Green Neurosurgery, 5(01), 44–47. https://doi.org/10.3126/egn.v5i01.68451

Issue

Section

Case Reports