Title: Dyke Davidoff Masson Syndrome- A Case Report

Authors: Sherry Garg, Sophia Garg

 DOI: https://dx.doi.org/10.18535/jmscr/v7i3.36

Abstract

Dyke Davidoff Mason syndrome is an uncommon childhood cerebral clinical entity. It is generally grouped into congenital and acquired. The congenital type is intrauterine type and acquired occurs in early life. We are here, presenting a case of 15 years old boy that came with chief complaint of 4 episodes of seizures and was accidentally diagnosed with this syndrome. He was subsequently treated with anticonvulsants and discharged.

References

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  3. Hageman G, Gooskens RHJM, Willememse J,A cerebral cause  of arthrogryposis: Unilateral cerebral hypoplasia. Clin Neurosurg1985; 87:s119-122
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Corresponding Author

Sophia Garg

Dr V M GMC Solapur

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