Results 31 to 40 of about 1,086 (191)
Dyke-Davidoff-Masson Syndrome in Pediatrics: Case Report of Atypical Status Epilepticus and Therapeutic Challenges in the Caribbean. [PDF]
Case Rep MedDyke–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]
J Dtsch Dermatol GesSummary 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
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
DYKE–DAVIDOFF–MASSON SYNDROME-A Rare Cause of Cerebral Hemiatrophy in a 17-Years-Old Ethiopian Patient: A Case Report [PDF]
, 2021 BACKGROUND: Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease with unknown frequency, mainly presented with seizures, facial asymmetry, contralateral hemiparesis and mental retardation. Often, resulting from brain injury due to a multitude of causes,
Alemayehu Ayele, Biniyam +1 more
core +2 more sources
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 +6 more
wiley +1 more source
Epilepsia Open, Volume 7, Issue 4, Page 810-816, December 2022., 2022 Abstract We describe a case of epileptic encephalopathy in a young woman with undiagnosed medium‐chain acyl‐coenzyme A dehydrogenase deficiency (MCADD), who presented with an early‐onset focal motor status epilepticus (SE) then followed by permanent left hemiplegia and drug‐resistant epilepsy with neurodevelopmental delay.
Ilaria Cani +13 more
wiley +1 more source
Clinical Outcome of Hypoglossal-Facial Nerve Anastomosis in Severe Facial Nerve Paralysis: An Experience from Khyber Pakhtunkhwa [PDF]
, 2022 Objectives: Facial nerve injury is one of the most devastating complications occurring as a result of any chemical, mechanical or ischemic insult.
Ramzan Hussain +5 more
core +2 more sources
Facial Hemiatrophy in a Monomania [PDF]
The Journal of Nervous and Mental Disease, 1883 n ...
openaire +1 more source
Dyke-Davidoff-Masson Syndrome as a rare congenital hemiatrophy: a case report: Dyke-Davidoff-Masson Syndrome [PDF]
, 2021 Introduction: Dyke-Davidoff-Masson syndrome (DDMS) is a rare condition in childhood with very few cases reported in sub-Saharan Africa. Typically, the patient presents with facial asymmetry, seizures, and hemiparesis.
Nwako, Azubuike Benjamin +3 more
core +1 more source