PT  - JOURNAL ARTICLE
AU  - Zawar, Ifrah
AU  - Khan, Ashfa A.
AU  - Sultan, Tipu
AU  - Rathore, Ahsan W.
TI  - Dyke-Davidoff-Masson Syndrome
AID  - 10.17712/nsj.2015.4.20150481
DP  - 2015 Oct 01
TA  - Neurosciences Journal
PG  - 385--387
VI  - 20
IP  - 4
4099  - http://nsj.org.sa/content/20/4/385.short
4100  - http://nsj.org.sa/content/20/4/385.full
SO  - Neurosciences (Riyadh)2015 Oct 01; 20
AB  - The Dyke-Davidoff-Masson Syndrome (DDMS) results from an insult to the growing brain in utero or early infancy, which lead to loss of neurons compromising the growth of the brain. Clinical presentation includes seizures, hemiparesis, facial asymmetry, and learning disability. Radiological findings include cerebral atrophy on one side. Here, we present a case with status epilepticus who had underlying DDMS. It is a rare syndrome and uncommon cause for status epilepticus. Infections of CNS, hypoxic ischemic encephalopathy, intracranial bleed, trauma, congenital vascular malformations are the common causes of this syndrome. Diagnosis is established after clinical history, examination, and MRI. Intractable seizures can be controlled with appropriate anticonvulsants. Subsequently, these children may require physiotherapy, speech therapy, and occupational therapy in addition to the anticonvulsant medication. Outcome is better if the seizures are controlled.