Results 21 to 30 of about 1,407 (200)

A rare case of Dyke-Davidoff-Masson syndrome with concurrent metabolic syndrome [PDF]

Radiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological condition resulting from prenatal or early childhood brain injury, characterized by seizures, hemiparesis, facial asymmetry, and intellectual disability, with imaging findings including cerebral
Sushmitha Rameshbabu, Naveenkumar Nallathambi, D Shaaruk, Imaduddin Mohammed, Neha Syed   +4 more
doaj   +2 more sources

Adult-onset generalized seizures in undiagnosed cerebral hemiatrophy: A case of Dyke-Davidoff-Masson syndrome [PDF]

Radiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS), is a rare neurological disorder commonly diagnosed in childhood which is characterized by cerebral hemiatrophy, leading to seizures, hemiparesis, and varying degrees of cognitive deficits.
Vipul K. Rathan, MBBS, MD, Gauri Malavalli Girish, MBBS, MD, Shreya H. Kalloli, MBBS, Jeco Jacob Kuttykandathil, MBBS, MD, Chakrapani Mahabala, MBBS, MD, Arfath Ahmed, MBBS, MD   +5 more
doaj   +2 more sources

Cerebral Hemiatrophy: Etiology and Pathology

Pediatric Neurology Briefs, 1991
Two types of cerebral hemiatrophy are reported from the Institute of Neuropathology at the University of Giessen, Arndtstrafse FRG.
J Gordon Millichap
doaj   +3 more sources

Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case [PDF]

Radiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS) is a rare entity. Few cases have been described in the literature. It can be symptomatic or asymptomatic. The clinical signs are very varied. Imaging is the key to diagnosis.
Nourrelhouda Bahlouli, Fatima Chait, Khadija Laasri, Yahya El Harras, Nazik Allali, Latifa Chat, Siham El Haddad   +6 more
doaj   +2 more sources

Dyke-Davidoff-Masson syndrome: A case report of an 11-year-old child managed for Erb's Palsy [PDF]

Radiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological anomaly encompassing clinical features of seizures, contralateral hemiparesis, facial asymmetry, and intellectual dysfunction.
Abdullah Javed, MBBS, Dawood Javed, MBBS
doaj   +2 more sources

Haberland Syndrome (Encephalocraniocutaneous Lipomatosis): A Case Report and Review of Literature. [PDF]

Iran J Child Neurol
Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland syndrome, is a rare, nonhereditary, nonprogressive congenital neurocutaneous syndrome with underlying ectodermal dysgenesis. The classic triad of this syndrome is central nervous system
Torabi A, Shervin Badv R, Mohammadpour M, Zamani F, Sadat Sadeghzadeh M, Pak N.   +5 more
europepmc   +3 more sources

Case Report: Dyke-Davidoff-Masson syndrome resulting from a rare combination of hypoplastic left posterior cerebral artery and ipsilateral fetal-type posterior communicating artery [PDF]

Frontiers in Human Neuroscience
IntroductionDyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder characterized by unilateral hemiparesis, facial asymmetry, severe epilepsy, and intellectual disability.
He Huang, Chunyu Wang, Huijuan Hua, Yingju Zhang, Bo Zhao, Dongjun Wan   +5 more
doaj   +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: A rare case of hemiatrophy of brain—Case report from Nepal

Radiology Case Reports, 2022
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder that results from brain injury during intrauterine or early years of life. Prominent cortical sulci, dilated lateral ventricles, cerebral hemiatrophy, hyperpneumatization of the sinus ...
Prakash Dhakal, MD, Suraj Sharma, MD, Abhishek Sharma, MBBS, Sajiva Aryal, MBBS, Seema Bhandari, MD   +4 more
doaj   +1 more source

Phenotypic Spectrum and Diagnostic Challenges in Klippel-Trenaunay Syndrome: A Case Series. [PDF]

Clin Case Rep
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.
Hameed M, Ali T, Haque MA.
europepmc   +2 more sources