Results 21 to 30 of about 2,008 (151)
Pansclerotic morphea: A male child with hemiatrophy of lower limb
Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and subcutaneous tissue. Pansclerotic morphea is a rare atrophying and sclerosing type of morphea. It can follow a comparatively benign course with spontaneous
Malay K Dasgupta +3 more
doaj +2 more sources
Adult Presentation of Dyke-Davidoff-Masson Syndrome, a Radiological Enigma: A Case Report. [PDF]
Introduction and Importance: Dyke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition characterized by focal or generalized drug‐resistant epilepsy, hemiparesis, face or body asymmetry with atrophy, and cognitive impairment in early childhood and adulthood. DDMS is generally diagnosed in the paediatric age group.
Paudel S +5 more
europepmc +2 more sources
Phenotypic Spectrum and Diagnostic Challenges in Klippel-Trenaunay Syndrome: A Case Series. [PDF]
ABSTRACT Klippel‐Trénaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, venous varicosities, and soft tissue or bony hypertrophy. This case series highlights rare and atypical presentations of KTS, emphasizing the importance of a multidisciplinary diagnostic approach.
Hameed M, Ali T, Haque MA.
europepmc +2 more sources
Localised Unilateral Facial Hemiatrophy
A very rare case of localized unilateral facial hemiatrophy is being presented here.
Gangopadhyay Asok +1 more
doaj +1 more source
Parry Romberg syndrome: A rare case report
The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam +3 more
doaj +2 more sources
Dyke-Davidoff-Masson syndrome: A case report
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 +2 more sources
A rare case of Dyke-Davidoff-Masson syndrome with concurrent metabolic syndrome [PDF]
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological condition resulting from prenatal or early childhood brain injury, characterized by seizures, hemiparesis, facial asymmetry, and intellectual disability, with imaging findings including cerebral
Sushmitha Rameshbabu +4 more
doaj +2 more sources
Natural History of Rasmussen’s Syndrome
Seizure frequency, degree of hemiparesis and cerebral hemiatrophy are analysed in 13 patients with histopathologically proven Rasmussen’s encephalitis (RE) examined at the University of Bonn, Germany.
J Gordon Millichap
doaj +2 more sources
Case report of progressive facial hemiatrophy
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 +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Trata-se de criança de oito anos, portadora de atrofia na hemiface direita, desde os seis anos. A ressonância magnética do encéfalo evidenciou espessamento cortical e formação de cistos.
Luciana Baptista Pereira +3 more
doaj +1 more source

