Results 71 to 80 of about 1,086 (191)

S2k guideline: Diagnosis and therapy of localized scleroderma

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.
Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter   +12 more
wiley   +1 more source

A case of Dyke-Davidoff-Masson syndrome [PDF]

open access: yes, 2012
Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis and mental retardation. The clinical findings may be of variable degree according to the extent of brain injury.
Ali Yikilmaz   +13 more
core   +1 more source

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

Pathophysiology of hemimasticatory spasm. [PDF]

open access: yes, 1994
Two patients aged 21 and 50 years presented with facial hemiatrophy and unilateral spasms of the masticatory muscles. Masticatory muscle biopsy showed normal findings in both patients and facial skin biopsy specimens only showed atrophy, although ...
Frisardi G   +8 more
core   +1 more source

Romberg′s Syndrome

open access: yesIndian Journal of Dermatology, 1999
A 16 year old female with facial hemiatrophy and convulsions having sparse right eyebrows and eye lashes, flattening of the nasolabial fold, protrusion of eye ball, and retraction of angle of mouth towards the affected side is reported.
Masuria B. L, Jain V. K, Kothiwala R. K
doaj  

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

Hemiatrofia facial progressiva (doença de Parry-Romberg): relato de dois casos associados a trigeminalgia e câimbras Progressive facial hemiatrophy (Parry-Romberg disease): report of two cases associated with trigeminal neuralgia and cramps [PDF]

open access: yes, 1997
Os autores relatam dois casos de hemiatrofia facial progressiva (HFP), ambos do sexo feminino, associados à hiperexcitabilidade neuromuscular, representada por dores neurálgicas e espasmos musculares (câimbras) numa hemiface.
Maurus Marques de Almeida Holanda   +3 more
core   +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

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