Results 101 to 110 of about 430,429 (236)
Prosthetic rehabilitation of an orbital defect for a patient with hemifacial atrophy
The 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
Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria [PDF]
, 2011 Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
Imarhiagbe, FA
core +1 more source
Case report of progressive facial hemiatrophy
Journal 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
Parry-Romberg syndrome with ipsilateral hemipons involvement presenting as monoplegic ataxia [PDF]
, 2015 ope
강훈철 +3 more
core +1 more source
, 2019 Bell’s palsy didefinisikan sebagai kelumpuhan saraf fasialis satu sisi, dengan penyebabnya tidak diketahui. Beberapa keadaan lain juga dapat menyebabkan kelumpuhan fasialis, misalnya tumor otak, stroke, myasthenia gravis, dan penyakit Lyme.
Adam, Olivia Mahardani
core +2 more sources
The Phakomatosis (Neurocutaneous Syndromes): Sturge-Weber Syndrome
مجله 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
Developmental malformations of human tongue and associated syndromes (review) [PDF]
, 2020 The development of the tongue begins as known, in the floor of the primitive oral cavity, when the human embryo is four weeks old.More specifically, the tongue develops from the region of the first three or four branchial arches during the period that ...
Emmanouil-Nikoloussi, E.-N +1 more
core +1 more source
Dyke-Davidoff-Masson Syndrome Following Head Trauma: Clinical and Radiologic Findings
Archives of EpilepsyDyke-Davidoff-Masson syndrome (DDM) is an unusual condition characterized by facial asymmetry, hemiparesis, mental retardation, learning disabilities, sensorineural hearing loss, psychiatric disorders, and epilepsy.
Muhittin Emre Altunrende +1 more
doaj +1 more source
Dyke-Davidoff-Masson Syndrome- a rare cause of refractory epilepsy.
Iranian Journal of Psychiatry, 2014 Dyke-Davidoff-Masson Syndrome (DDMS) is a syndrome associated with refractory epilepsy. DDMS is a rare syndrome characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation.
Prerna Malik +3 more
doaj
Síndrome de Romberg: uma série de casos
Revista Brasileira de Cirurgia PlásticaINTRODUÇÃO: A síndrome de Romberg é uma moléstia descrita há mais de um século e, nesse período, recebeu várias denominações. É caracterizada por lenta e progressiva atrofia dos tecidos de uma hemiface, podendo acometer todos os tecidos e apresentar ...
Isis Juliane Guarezi Nasser +8 more
doaj +1 more source