Results 31 to 40 of about 1,412 (198)

Síndrome Dyke Davidoff Masson Aspectos Clínico-Radiológicos: Reporte de Caso [PDF]

open access: yes, 2021
Background: Dyke Davidoff Masson syndrome (DDM) is a rare entity. This syndrome has a variable clinical presentation from mild to severe cases, which is why it constitutes a diagnostic challenge at an early age and for treating personnel. However, within
Avellaneda, Luis Carlos   +2 more
core   +2 more sources

Dyke Davidoff Masson Syndrome with Abdominal Epilepsy-Rare Presentation

open access: yesAsian 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

Progressive hemifacial atrophy Parry Romberg syndrome characteristics of craniofacial morphology [PDF]

open access: yesStomatološki glasnik Srbije, 2007
The aim of this case report was to analyze clinical finding in a patient with rare, Parry Romberg syndrome. The patient was diagnosed with progressive facial hemiatrophy that affected skin, subcutaneous tissue and underlying bony structures.
Nikodijević-Latinović Angelina
doaj   +1 more source

Dyke-Davidoff-Masson syndrome: A case report with a literature review

open access: yesRadiology 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]

open access: yes, 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]

open access: yes, 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

open access: yesMedical 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

Facial Hemiatrophy in a Monomania [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1883
n ...
openaire   +1 more source

Síndrome de moyamoya associada a neurofibromatose tipo I em paciente pediátrico [PDF]

open access: yes, 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
core   +1 more source

Facioscapulohumeral muscular dystrophy: more complex than it appears [PDF]

open access: yes, 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

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