Literature DB >> 24419451

Crossed cerebro-cerebellar atrophy with Dyke Davidoff Masson syndrome.

Hussein A Algahtani1, Ahmed A Aldarmahi, Mohammed W Al-Rabia, G Bryan Young.   

Abstract

Dyke Davidoff Masson syndrome (DDMS) refers to atrophy or hypoplasia of one cerebral hemisphere following a prior fetal or childhood insult. It has characteristics of clinical and radiological changes. These changes include hemiparesis, seizures, facial-asymmetry, and mental retardation. We present a 25-year-old man with crossed cerebrocerebellar atrophy and DDMS. His seizures were well controlled using a combination of antiepileptic drugs.

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Year:  2014        PMID: 24419451

Source DB:  PubMed          Journal:  Neurosciences (Riyadh)        ISSN: 1319-6138            Impact factor:   0.906


  3 in total

1.  Dyke-Davidoff-Masson syndrome in a Nigerian.

Authors:  Philip B Adebayo; Amnat Bakare; Modupe M Bello; Opeyemi D Olaewe; Kolawole W Wahab
Journal:  Epilepsy Behav Case Rep       Date:  2016-09-15

2.  Magnetic resonance imaging depiction of acquired Dyke-Davidoff-Masson syndrome with crossed cerebro-cerebellar diaschisis: Report of two cases.

Authors:  Ranjana Gupta; Sandeep Joshi; Amit Mittal; Ishita Luthra; Puneet Mittal; Vibha Verma
Journal:  J Pediatr Neurosci       Date:  2015 Jul-Sep

3.  Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report.

Authors:  Ujjawal Roy; Ajay Panwar; Adreesh Mukherjee; Debsadhan Biswas
Journal:  Case Rep Neurol       Date:  2016-01-16
  3 in total

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