Results 11 to 20 of about 71,603 (162)

Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy

South African Journal of Radiology, 2017
Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar, Shishir Chauhan, Abhijit M. Patil, Siddappa G. Gandage, Surbhi Chauhan Kalra   +4 more
doaj   +3 more sources

Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report

Case Reports in Neurology, 2016
Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy, Ajay Panwar, Adreesh Mukherjee, Debsadhan Biswas   +3 more
doaj   +2 more sources

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

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

Communicating Hydrocephalus in a Case of Long-Term Primary Hyperparathyroidism [PDF]

Journal of the ASEAN Federation of Endocrine Societies, 2018
We present the rare case of a 47-year-old woman with protracted primary hyperparathyroidism complicated by communicating hydrocephalus and cerebellar tonsillar herniation secondary to calvarial thickening. The parathyroid glands remained elusive, despite
Cheow Peng Ooi, Norlaila Mustafa, Thean Yean Kew   +2 more
doaj   +2 more sources

Traumatic Sinus Pericranii Managed Surgically: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Sinus pericranii is a rare venous anomaly characterized by abnormal communication between extracranial veins and intracranial dural venous sinuses. Traumatic sinus pericranii is uncommon. We report a 35‐year‐old man who presented with a progressively enlarging scalp mass 8 years after head trauma.
Asadi S, Iranmehr A, Shirani M, Rohani A.   +3 more
europepmc   +2 more sources

Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation-Region Frameshift Variant. [PDF]

Mol Genet Genomic Med
A novel KRIT1 initiation‐region frameshift variant, NM_004912.4.2dup [p.(Met1IlefsTer31)], was identified in a pediatric family with familial cerebral cavernous malformation. Marked intrafamilial variability supports early molecular diagnosis, cascade family screening, and susceptibility‐sensitive MRI surveillance. ABSTRACT Background Familial cerebral
Yayıcı Köken Ö, Yanartaş MS, Aygün H, Ceylan AC, Karaali K, Kazan MS.   +5 more
europepmc   +2 more sources

Acquired Chiari Type 1 Malformation Secondary to Paget’s Disease of the Bone: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2021
Chiari type 1 malformations are characterised by caudal descent of cerebellar tonsil into foramen magnum. Usually it is congenital. Paget’s disease causing acquired chiari type 1 malformation is rare with only five reported cases in the literature.
Srestha Khan, Senthil Kumar Aiyappan, Abinesh Govindarajan, Vinayagam Shanmugam   +3 more
doaj   +1 more source

Radiographic analysis of the thickness of the cranial bones in captive compared to wild-living cheetahs and in cheetahs with hypovitaminosis A

PLoS ONE, 2021
Captive cheetahs often demonstrate a high incidence of diseases in which vitamin A imbalances are implicated. These can occur even under controlled and optimised feeding regimens, which is why surveillance of vitamin A status is mandatory in the ...
Martin J. Schmidt, Gerhard Steenkamp, Peter Caldwell, Klaus Failing, Robert M. Kirberger   +4 more
doaj   +2 more sources

CALVARIAL THICKENING AFTER DILANTIN MEDICATION [PDF]

American Journal of Roentgenology, 1970
Increase in the thickness of the calvaria, mainly in the diploic space, was noticed in epileptic patients receiving dilantin for prolonged periods. The younger the patient, the more prominent were the changes. Three white teenage patients are reported with skull roentgenograms before and 3 or more years after the institution of dilantin medication.
openaire   +2 more sources

Primary Calvarial Tuberculosis Presenting with Scalp Swelling and Lytic Bone Lesion: A Case Report [PDF]

, 2018
Calvarial tuberculosis is a rare entity in developed countries. Even though it is a rare occurrence, the incidence of calvarial tuberculosis is increasing in developed countries because of migration from developing countries with poor socio-economic ...
Murat Koçyiğit, Uzay Erdoğan, Aykut Akpınar   +2 more
core   +1 more source