Results 41 to 50 of about 430,429 (236)

Parry Romberg Syndrome with localized scleroderma: a case report [PDF]

open access: yes, 2014
Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Gupta, Nikita   +3 more
core   +1 more source

DYKE–DAVIDOFF–MASSON SYNDROME-A Rare Cause of Cerebral Hemiatrophy in a 17-Years-Old Ethiopian Patient: A Case Report [PDF]

open access: yes, 2021
BACKGROUND: Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease with unknown frequency, mainly presented with seizures, facial asymmetry, contralateral hemiparesis and mental retardation. Often, resulting from brain injury due to a multitude of causes,
Alemayehu Ayele, Biniyam   +1 more
core   +2 more sources

FACIAL HEMIATROPHY [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1916
n ...
openaire   +1 more source

Scleroderma and dentistry: Two case reports [PDF]

open access: yes, 2016
© 2016 The Author(s).Background: Scleroderma is a chronic connective tissue disorder with unknown etiology. It is characterized by excessive deposition of extracellular matrix in the connective tissues causing vascular disturbances which can result in ...
Bornstein, Michael M.   +4 more
core   +1 more source

Idiopathic hemifacial atrophy successfully treated with hyaluronic acid filler: About two new cases

open access: yes, 2023
Journal of Cosmetic Dermatology, Volume 22, Issue 3, Page 1142-1145, March 2023.
Kouki Chaima   +2 more
wiley   +1 more source

Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy

open access: yesSouth African Journal of Radiology, 2017
Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar   +4 more
doaj   +1 more source

Orofacial myofunctional characterization in Parry-Romberg syndrome [PDF]

open access: yes, 2015
Objetivo: Caracterizar os aspectos miofuncionais orofaciais de pacientes acometidos pela síndrome de Parry-Romberg, por meio de protocolos clínicos padronizados e da Eletromiografia de Superfície (EMGs) dos músculos mastigatórios.
Andrade, Claudia Regina Furquim de   +3 more
core   +1 more source

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

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