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Dyke-Davidoff-Masson syndrome: A case report with a literature review
Radiology Case Reports, 2022 Dyke-Davidoff-Masson syndrome (DDMS) is an uncommon neurological disease defined as cerebral hemiatrophy with a contralateral motor deficit, facial asymmetry, and seizures.
Mohamed Hamid, MD +3 more
doaj +1 more source
Autologous fat grafting in facial volumetric restoration [PDF]
, 2015 The authors reported their surgical experience about structural fat grafting in the management of facial volumetric deficit. The purpose of this study was to assess the real indications, cosmetic results, complications, and global patient satisfaction of
Dell'Aversana orabona , Giovanni +4 more
core +1 more source
Trudności diagnostyczne objawów napadowych u chłopca z zespołem Parry'ego-Romberga [PDF]
, 1970 Parry-Romberg syndrome is characterized by progressive unilateral facial atrophy affecting subcutaneous tissue, cartilage and bone structures. Headache attacks and epilepsy are commonly associated with this syndrome but the underlying pathophysiology is ...
Biedroń, Agnieszka +3 more
core +5 more sources
Dyke-Davidoff-Masson syndrome: A case report
Medical Journal of Dr. D.Y. Patil University, 2014 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.
Biswajyoti Rath +3 more
doaj +1 more source
Síndrome de moyamoya associada a neurofibromatose tipo I em paciente pediátrico [PDF]
, 2011 CONTEXT: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder among humans. Moyamoya disease is a cerebral vasculopathy that is only rarely observed in association with NF-1, particularly in the pediatric age range ...
DARRIGO JÚNIOR, Luiz Guilherme +5 more
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Facioscapulohumeral muscular dystrophy: more complex than it appears [PDF]
, 2014 Facioscapulohumeral muscular dystrophy (FSHD) has been classified as an autosomal dominant myopathy, linked to rearrangements in an array of 3.3 kb tandemly repeated DNA elements (D4Z4) located at the 4q subtelomere (4q35).
RICCI, GIULIA, TUPLER, Rossella, Zatz, M
core +1 more source
Neurodevelopmental abnormalities in children with PHACE syndrome. [PDF]
, 2012 Prior case reports have identified neurodevelopmental abnormalities in children with PHACE syndrome, a neurocutaneous disorder first characterized in 1996.
Barkovich, A James +8 more
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Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease [PDF]
, 2017 OBJECTIVES: To analyse and describe the clinical and genetic spectrum of Charcot-Marie-Tooth disease (CMT) caused by mutations in the neurofilament light polypeptide gene (NEFL).
Bettencourt, C +18 more
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Dysmorphometrics: the modelling of morphological abnormalities [PDF]
, 2012 BACKGROUND: The study of typical morphological variations using quantitative, morphometric descriptors has always interested biologists in general. However, unusual examples of form, such as abnormalities are often encountered in biomedical sciences ...
Dirk Vandermeulen +5 more
core +2 more sources
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 +3 more
doaj +1 more source