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

