Autor: |
Biswajyoti Rath, Maheswar Samant, Kali P Swain, Ashok K Mallick |
Jazyk: |
angličtina |
Rok vydání: |
2014 |
Předmět: |
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Zdroj: |
Medical Journal of Dr. D.Y. Patil University, Vol 7, Iss 5, Pp 672-674 (2014) |
Druh dokumentu: |
article |
ISSN: |
0975-2870 |
DOI: |
10.4103/0975-2870.140494 |
Popis: |
Dyke-Davidoff-Masson Syndrome (DDMS), also called as cerebral hemiatrophy, is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties. It is commonly diagnosed in presence of associated radiologic findings, which include cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. We present a 21-year female with increased frequency of convulsion and abnormal behavior for the last 2 months. She had a known seizure disorder for 15 years and had mental subnormality. On physical examination, she was disoriented with mild right hemiparesis. On CT scan the brain showed unilateral left cerebral atrophy. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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