Results 31 to 40 of about 1,463 (166)
Pansclerotic morphea: A male child with hemiatrophy of lower limb
Indian Dermatology Online Journal, 2014 Morphea is a variant of localized scleroderma in which lesions are usually limited to the skin and subcutaneous tissue. Pansclerotic morphea is a rare atrophying and sclerosing type of morphea. It can follow a comparatively benign course with spontaneous
Malay K Dasgupta +3 more
doaj +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2007 Trata-se de criança de oito anos, portadora de atrofia na hemiface direita, desde os seis anos. A ressonância magnética do encéfalo evidenciou espessamento cortical e formação de cistos.
Luciana Baptista Pereira +3 more
doaj +1 more source
Dyke Davidoff Masson Syndrome with Abdominal Epilepsy-Rare Presentation
Asian Journal of Medical Sciences, 2013 Dyke Davidoff Masson Syndrome (DDMS) with abdominal epilepsy, is a rare clinical condition. It is characterized by severe abdominal pain with seizures, facial asymmetry, contralateral hemiparesis, and mental retardation.
Shitanshu Srivastava
doaj +1 more source
Seizures in patients with cerebral hemiatrophy: A prognostic evaluation
Annals of Indian Academy of Neurology, 2015 Purpose: Cerebral hemiatrophy is a common childhood disease. It clinically manifests with seizures, hemiparesis and mental retardation. Materials and Methods: In this prospective study, previously untreated patients with seizures and cerebral hemiatrophy
Anupam Jaiswal +4 more
doaj +1 more source
Dyke-Davidoff-Masson Syndrome Following Head Trauma: Clinical and Radiologic Findings
Archives of EpilepsyDyke-Davidoff-Masson syndrome (DDM) is an unusual condition characterized by facial asymmetry, hemiparesis, mental retardation, learning disabilities, sensorineural hearing loss, psychiatric disorders, and epilepsy.
Muhittin Emre Altunrende +1 more
doaj +1 more source
Birth Defects Research, Volume 118, Issue 6, June 2026.ABSTRACT Background Hemifacial microsomia (HFM) is a congenital craniofacial malformation characterized by unilateral hypoplasia of structures derived from the first and second pharyngeal arches. Although the phenotype is well described, the underlying etiology remains incompletely understood.
Karl Jacobs +7 more
wiley +1 more source
CT of cerebral hemiatrophy [PDF]
American Journal of Roentgenology, 1980 Computed tomography (CT) findings in 10 cases of cerebral hemiatrophy are described. The CT appearance is typical and reflects the pathologic changes of unilateral loss of brain substance and calvarial thickening. In four patients with a mild form of the disease, a correct analysis of the pain skull radiographs was made only in retrospect. CT was found
openaire +2 more sources
Amygdala enlargement associated with remote epileptogenic lesions
Epilepsia, Volume 67, Issue 5, Page 2389-2399, May 2026.Abstract Objective To determine the prevalence and possible causes of amygdala enlargement in patients with drug‐resistant temporal lobe epilepsy. Methods Patients were retrospectively identified via a radiology information system and a large language model.
Horst Urbach +5 more
wiley +1 more source
Dyke-Davidoff-Masson syndrome: A case report
Medical Journal of Dr. D.Y. Patil University, 2014 Dyke-Davidoff-Masson Syndrome (DDMS), also called as cerebral hemiatrophy, is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties.
Biswajyoti Rath +3 more
doaj +1 more source