Results 21 to 30 of about 276,835 (194)

Progressive Facial Hemiatrophy. [PDF]

Dtsch Arztebl Int
Makhlouf S.
europepmc   +3 more sources

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

Clin 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, Majeed HM, Farooqi HH, Khaliq MW, Chohan DA, Mushtaq A, Gohar A, Ahmad MH.   +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]

Clin 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

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

J Cosmet Dermatol
Journal of Cosmetic Dermatology, Volume 24, Issue 5, May 2025.
Gomez-Martinez S, Fuertes I, Ferrer Fuertes A, Gonzalez FJC, Martí Pagés C, Lledó-Ibáñez GM, Espinosa G, Quintana-Codina M, Iglesias Sancho M, Cembrano MD, Bosch-Amate X, Mascaró JM, Giavedoni P.   +12 more
europepmc   +2 more sources

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

Clin 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, Duhan A, Al-Taie RH, Abbas AH, Abdulgadir A, Khalil I, Bacha Z, Al-Gizey N.   +7 more
europepmc   +2 more sources

Adult Presentation of Dyke-Davidoff-Masson Syndrome, a Radiological Enigma: A Case Report. [PDF]

Case 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, Acharya A, Pokharel R, Rokaha PS, Rokaha PS, Luitel A.   +5 more
europepmc   +2 more sources

DYKE-DAVIDOFF-MASSON SYNDROME [PDF]

National Journal of Medical Research, 2013
Dyke-Davidoff-Masson Syndrome (DDMS) is characterized by Seizures, facial asymmetry, contralateral hemiplegia and Mental Retardation. Characteristic Radiological features are Cerebral hemiatrophy with homolateral hypertrophy of skull and sinuses?
Sasi Sekhar T V D, Satish P, Krishnaveni Vanapala, Anvesh Golla   +3 more
doaj   +1 more source

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

Case 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, Lucas-Muñoz D, Colomé-Hidalgo M, Vásquez-Gómez G.   +3 more
europepmc   +2 more sources

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

American 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

Noninvasive imaging exploration of phacomatosis pigmentokeratotica using high‐frequency ultrasound and optical coherence tomography: Can biopsy of PPK patients be avoided?

Skin Research and Technology, Volume 29, Issue 4, April 2023., 2023
Abstract Background Phacomatosis pigmentokeratotica (PPK) is a distinct and rare type of epidermal nevus syndrome characterized by coexisting nonepidermolytic organoid sebaceous nevus (SN) with one or more speckled lentiginous nevi (SLN). Atypical nevi including compound Spitz and compound dysplastic may manifest within regions of SLN.
Jenna Lee, Juliana Benavides, Rayyan Manwar, Carolina Puyana, Julia May, Maria Tsoukas, Kamran Avanaki   +6 more
wiley   +1 more source