Results 11 to 20 of about 920 (168)

Dyke-Davidoff-Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder. [PDF]

open access: yesClin Case Rep
ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Shafiq W   +7 more
europepmc   +2 more sources

Dyke-Davidoff-Masson Syndrome in a Female Adult: A Rare Case of Progressive Hemiparesis, Epilepsy, and Cerebral Hemiatrophy. [PDF]

open access: yesClin Case Rep
ABSTRACT Consideration of Dyke‐Davidoff‐Masson syndrome (DDMS) in patients with epilepsy, hemiparesis, and cognitive impairment should be taken into account. MRI plays a key role in diagnosing this rare disorder by recognizing cerebral hemiatrophy with compensatory skull and sinus hypertrophy.
La QD, Baloch A, Ayub M, Ahmed S, Lue E.
europepmc   +2 more sources

Case Report of Rasmussen's Encephalitis With a Decade of Refractory Epilepsy and Hemispheric Atrophy. [PDF]

open access: yesClin Case Rep
ABSTRACT Rasmussen's encephalitis (RE) is a rare, chronic inflammatory neurological disorder affecting one cerebral hemisphere and presenting with drug‐resistant epilepsy, progressive hemiparesis, and cognitive decline. This case report describes the clinical course and management of a 21‐year‐old patient with refractory epilepsy and progressive ...
Al-Badri S   +7 more
europepmc   +2 more sources

High-Frequency Ultrasound Assessment of Skin Thickness Following Lipofilling in Facial Sclerosing Dermatoses: A Case Series. [PDF]

open access: yesJ Cosmet Dermatol
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Gomez-Martinez S   +12 more
europepmc   +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

Dyke-Davidoff-Masson Syndrome in Pediatrics: Case Report of Atypical Status Epilepticus and Therapeutic Challenges in the Caribbean. [PDF]

open access: yesCase Rep Med
Dyke–Davidoff–Masson syndrome (DDMS), also known as cerebral hemiatrophy, is characterized by brain damage resulting in hypoplasia of one cerebral hemisphere. It is described as a rare disorder, primarily characterized by epileptic seizures and convulsions, as well as hemiparesis and cognitive impairments.
Martín-Sanz MB   +3 more
europepmc   +2 more sources

Sclerosing diseases of the skin. [PDF]

open access: yesJ Dtsch Dermatol Ges
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Kalantari Y   +4 more
europepmc   +2 more sources

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

Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 192, Issue 3-4, Page 41-52, April-June 2023., 2023
Abstract Four years before the rediscovery of Mendel's work in 1900, Karl Grassmann published a detailed, scholarly review of the heredity of psychosis which we here review. A full translation is in the appendix. We emphasize seven major conclusions from this review.
Kenneth S. Kendler, Astrid Klee
wiley   +1 more source

Facial hemihypertrophy and facial hemiatrophy: Report of 2 cases

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2008
Facial hemihypertrophy and facial hemiatrophy are rare developmental anomalies. These conditions are characterized by an asymmetric growth of one or more parts of the tissues on one side of the face. The facial asymmetry may be total or partial.
Atul Indurkar   +2 more
doaj   +1 more source

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