Results 21 to 30 of about 2,008 (151)

Pansclerotic morphea: A male child with hemiatrophy of lower limb

open access: yesIndian Dermatology Online Journal, 2014
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]

open access: yesCase Rep Radiol
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]

open access: yesClin Case Rep
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

open access: yesIndian Journal of Dermatology, 2002
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

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2014
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

open access: yesMedical Journal of Dr. D.Y. Patil University, 2014
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]

open access: yesRadiology Case Reports
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

open access: yesPediatric Neurology Briefs, 2002
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

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   +1 more source

Você conhece esta síndrome? Do you know this syndrome?

open access: yesAnais Brasileiros de Dermatologia, 2007
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

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