Results 51 to 60 of about 276,835 (194)
Dyke-Davidoff-Masson Syndrome: A Case Report
International Journal of Medical Students, 2022 Background: Dyke-Davidoff-Masson syndrome (DDMS) is a neurological syndrome characterized by the presence of convulsions, facial asymmetry due to palsy of the facial nerve (CN VII), contralateral hemiplegia, and reduced intellectual capacity. The Case:
Gaurav M. Urs, Hitesh R. Doddabele
doaj +1 more source
Phenotypic Spectrum and Diagnostic Challenges in Klippel‐Trenaunay Syndrome: A Case Series
Clinical Case Reports, Volume 13, Issue 11, November 2025.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.
Marya Hameed, Tooba Ali, Md Ariful Haque
wiley +1 more source
Epidermal Nevi and Epidermal Naevus Syndromes
JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini +2 more
wiley +1 more source
Dyke-Davidoff-Masson syndrome presenting with recurrent seizures [PDF]
Romanian Journal of Neurology, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is cerebral hemiatrophy occurring following brain insult resulting from infarct, trauma or infection in utero or soon after birth.
M. Rajaguru +4 more
doaj +1 more source
Ellis-van Creveld syndrome with facial hemiatrophy
, 2010 Ellis-van Creveld (EVC) syndrome is a rare autosomal recessive congenital disorder characterized by chondrodysplasia and polydactyly, ectodermal dysplasia and congenital defects of the heart.
Bhat, Yasmeen J. +5 more
core +1 more source
Indian Journal of Dermatology, 2001 A case of Facial Hemiatrophy is being reported for its rarity and clinical interest.
Baishampayan S +3 more
doaj
Epilepsia, Volume 65, Issue 12, Page 3607-3618, December 2024.Abstract Objective High‐field magnetic resonance imaging (MRI) is a standard in the diagnosis of epilepsy. However, high costs and technical barriers have limited adoption in low‐ and middle‐income countries. Even in high‐income nations, many individuals with epilepsy face delays in undergoing MRI.
Tobias Bauer +15 more
wiley +1 more source
Przegląd Dermatologiczny, 2011 Introduction. Progressive facial hemiatrophy (Parry-Romberg syndrome)is a relatively rare disease of unclear aetiology. Some authorspostulate its relation with linear scleroderma.Objective.
Ligia Brzezińska-Wcisło +2 more
doaj
Autoimmune‐associated seizure disorders
Epileptic Disorders, Volume 26, Issue 4, Page 415-434, August 2024.Abstract With the discovery of an expanding number of neural autoantibodies, autoimmune etiologies of seizures have been increasingly recognized. Clinical phenotypes have been identified in association with specific underlying antibodies, allowing an earlier diagnosis.
Kelsey M. Smith +7 more
wiley +1 more source
Anatomy of Aging Facial Skeleton
, 2021 The facial lifting or rhytidoplasty is a technique for ideal treatment of facial aging. To provide a jovial result, it is necessary to correct and reposition the anatomical structures without changing the naturalness of the face.
Mazzetti, Marcelo Paulo Vaccari +3 more
core +1 more source