Results 41 to 50 of about 920 (168)

Adult Presentation of Dyke Davidoff Masson Syndrome With Schizoaffective Disorder — A Case Report

open access: yesKerala Journal of Psychiatry, 2018
Dyke Davidoff Masson syndrome (DDMS) is a rare disease with characteristic radiological features, seizures, mental retardation, facial asymmetry, and psychiatric manifestations. Here, we report a case of a 50-year-old female who had a refractory seizure
MK Dinesh Kumar, Denver Steven Pinto
doaj   +1 more source

Phenotypic Spectrum and Diagnostic Challenges in Klippel‐Trenaunay Syndrome: A Case Series

open access: yesClinical 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

Neurodevelopmental influences in psychosis: a case of left cerebral hemiatrophy and schizoaffective disorder

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
Cerebral hemiatrophy (or Dyke-Davidoff-Masson Syndrome) is a neurodevelopmental disorder characterized by atrophy or hypoplasia of one cerebral hemisphere accompanied by ipsilateral calvarial changes.
Asli Demirtas Tatlidede   +2 more
doaj   +1 more source

Acquired Dyke-Davidoff-Masson syndrome (DDMS)

open access: yesInternational Journal of Advanced Medical and Health Research, 2015
Dyke-Davidoff-Masson syndrome (DDMS) is characterized by cerebral hemiatrophy, contralateral hemiplegia, skull and facial asymmetries, seizures, and mental retardation. We present a case of acquired DDMS following meningoencephalitis.
Jitender Aneja   +3 more
doaj   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

open access: yesJEADV 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

Localised Unilateral Facial Hemiatrophy

open access: yesIndian Journal of Dermatology, 2002
A very rare case of localized unilateral facial hemiatrophy is being presented here.
Gangopadhyay Asok   +1 more
doaj  

Dyke-Davidoff-Masson syndrome presenting with recurrent seizures [PDF]

open access: yesRomanian 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

Two Cases of Dyke-Davidoff Masson Syndrome

open access: yesArchives of Epilepsy, 2017
Dyke-Davidoff Masson Syndrome (DDMS) is a rare syndrome characterized by seizures, facial asymmetry, and contralateral hemiplegia or hemiparesis. The typical radiological features of DDMS include cerebral hemiatrophy with ipsilateral hypertrophy of the ...
Sabiha TEZCAN   +4 more
doaj   +1 more source

Facial Heamiatrophy

open access: yesIndian Journal of Dermatology, 2001
A case of Facial Hemiatrophy is being reported for its rarity and clinical interest.
Baishampayan S   +3 more
doaj  

Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report

open access: yesArquivos de Neuro-Psiquiatria, 1995
Os autores apresentam o caso de uma paciente de 45 anos de idade com história de 15 meses de evolução, de hemiatrofia progressiva da face e língua à esquerda.
Nicandro De Figueiredo Neto   +3 more
doaj   +1 more source

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