Results 51 to 60 of about 844,102 (172)

Dyke Davidoff syndrome: a rare cause of cerebral hemiatrophy in 11 months old

International Journal of Contemporary Pediatrics, 2020
Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon condition, characterized radiologically by cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses, of unknown frequency resulting from brain injury due to large no of causes ...
Amit J. Vatkar, Ipsita Vashishtha, Vinaykumar P Hedaginal, B. Madhav   +3 more
semanticscholar   +1 more source

A case of partial anomalous systemic venous drainage and perioperative detection of cerebral arteriovenous malformations

Annals of Pediatric Cardiology, 2021
We report a case of 8-year-old boy with unexplained desaturation and clubbing. Echocardiography showed anomalous drainage of right superior vena cava into left atrium. He did not have any neurological symptoms preoperatively.
Nilanjan Dutta, Debasis Das, Raghu Maruti Govindappa, Patralekha Das, Rangan Koley, Manish Kumar Sharma, Amitabha Chattopadhyay, Sanjiban Ghosh   +7 more
doaj   +1 more source

Neurodevelopmental Influences in Psychosis: A Case of Left Cerebral Hemiatrophy and Schizoaffective Disorder

Journal of Microbiology and Biotechnology, 2013
Ayse Destina Yalcin
exaly   +2 more sources

Dyke Davidoff Masson Syndrome with Abdominal Epilepsy-Rare Presentation

Asian Journal of Medical Sciences, 2013
Dyke Davidoff Masson Syndrome (DDMS) with abdominal epilepsy, is a rare clinical condition. It is characterized by severe abdominal pain with seizures, facial asymmetry, contralateral hemiparesis, and mental retardation.
Shitanshu Srivastava
doaj   +1 more source

Hemiparkinsonism or Hemidystonia With Hemiatrophy Syndrome: A Case Series With Follow-Up

Frontiers in Neuroscience, 2020
Hemiparkinsonism-hemiatrophy syndrome (HPHA) and hemidystonia-hemiatrophy syndrome (HDHA) are rare movement disorders composed of hemidystonia or hemiparkinsonism that present with unilateral limb, face, trunk, or cerebral hemiatrophy and mostly occur ...
Chentao He, Piao Zhang, Yan Li, Bing Li, Zhiheng Huang, Lijuan Wang, Yuhu Zhang   +6 more
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: An endocrine perspective [PDF]

Romanian Medical Journal, 2020
Dyke-Davidoff-Masson syndrome (DDMS) represents a severe disease that is caused by brain anomalies of different mechanisms early in life during fetal period or within first years after birth.
Cristina Dumitrescu, Anda Dumitrascu, Corina Chirita, Eugenia Petrova, Nicoleta Dumitru, Adina Ghemigian, Mara Carsote, Dana Terzea, Ana Valea   +8 more
doaj   +1 more source

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

Case Reports in Neurology, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy, Ajay Panwar, Adreesh Mukherjee, Debsadhan Biswas   +3 more
doaj   +1 more source

MR and CT imaging in the Dyke-Davidoff-Masson syndrome: report of three cases and contribution to pathogenesis and differential diagnosis [PDF]

Arquivos de Neuro-Psiquiatria, 1998
Cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis, and mental retardation.
PAULO HENRIQUE AGUIAR, WEI LIU CHING, HELIO LEITÃO, F. ISSA, GUILHERME LEPSKI, EBERVAL GADELHA FIGUEIREDO, FERNANDO GOMES-PINTO, RAUL MARINO JR   +7 more
doaj   +1 more source

When Asymmetry is the rule only Dyke & Davidoff Can Help An Interesting Case of Cerebral Hemiatrophy (Clinical Image)

, 2020
Here we present an interesting case of hemiatrophy of the brain resulting from any insult to the growing brain, which leads to corresponding phenotypic manifestations in the body.
M. Suhas
semanticscholar   +1 more source

Natural History of Rasmussen’s Syndrome

Pediatric Neurology Briefs, 2002
Seizure frequency, degree of hemiparesis and cerebral hemiatrophy are analysed in 13 patients with histopathologically proven Rasmussen’s encephalitis (RE) examined at the University of Bonn, Germany.
J Gordon Millichap
doaj   +1 more source