Results 61 to 70 of about 920 (168)

Dyke-Davidoff-Masson Syndrome

open access: yesJournal of Nobel Medical College, 2012
Dyke-Davidoff-Masson Syndrome (DDMS) is characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation. The characteristic radiologic features are cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses ...
Naba Raj Koirala   +5 more
doaj   +1 more source

Facial hemiatrophy: Review of literature and a case report

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2011
A case report of hemifacial atrophy is presented in this paper. It is also known as Parry-Romberg syndrome, is an uncommon degenerative and poorly understood condition.
Manisha S Tijare   +4 more
doaj   +1 more source

Parry-romberg syndrome: about a case

open access: yesThe Pan African Medical Journal, 2017
A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations
Hanane Oummad, Lalla Ouafae Cherkaoui
doaj   +1 more source

PARRY-ROMBERG SYNDROME

open access: yesRevista Ciencias Biomédicas, 2015
Introduction: the progressive hemifacial atrophy or Parry-Romberg syndrome is a rare disease, of slow clinical evolution that generates atrophy of the soft tissues.
Redondo-Bermúdez César   +4 more
doaj  

Progressive facial and cerebral hemiatrophy

open access: yesCleveland Clinic Journal of Medicine, 1984
A 43-year-old woman with progressive facial hemiatrophy had contralateral hemianopia and sensory loss. A computed-tomographic brain scan showed ipsilateral cerebral atrophy. The neurological and neuroradiological features of progressive facial hemiatrophy are reviewed.
openaire   +2 more sources

Prosthetic rehabilitation of an orbital defect for a patient with hemifacial atrophy

open access: yesThe Journal of Indian Prosthodontic Society, 2016
Removal of an eye may be indicated in cases of congenital abnormality, severe trauma, or disease such as an infection, tumor, or malignancy. The disfigurement associated with a loss of an eye is often accompanied with physical problems, psychological ...
Sanath Shetty   +3 more
doaj   +1 more source

ePoster

open access: yes
European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Case report of progressive facial hemiatrophy

open access: yesJournal of Holistic Nursing and Midwifery, 2007
Introduction: Progressive facial hemiatrophy (Parry-Romberg syndrome) is a rare disease ‎always with neurological symptoms such as migraine and epilepsy.
tahereh seyednoori   +2 more
doaj  

The Phakomatosis (Neurocutaneous Syndromes): Sturge-Weber Syndrome

open access: yesمجله دانشکده پزشکی اصفهان, 2008
Neurocutaneous syndromes or phakomatosis are inherited or sporadic conditions that feature lesions of both skin and nervous system. Sturge-weber syndrome (SWS) is characterized by a facial cutaneaous angioma (port-wine nevus) and an associated ...
Ahmad Chitsaz
doaj  

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