نتایج جستجو برای: brain malformation

تعداد نتایج: 486518  

Journal: :iranian journal of neuro surgery 0
آندرآ بوچی andrea boschi university of florence, florence, italy جیووانی بربگلی giovanni barbagli department of neurosurgery, university of florence, italy, via dante da castiglione 33, 50125, florence, italy بهمن اشرف نوبری bahman ashraf-noubari ادواردو سیپولچی edvardo cipolleschi سالواتوره مانجیافیکو salvatore mangiafico فرانکو آماناتی franco ammannati

background & importance: our study was performed based on the first case, reported in english, of a patient with three contemporary lesions, an extra-axial malformation and two vascular ones. case presentation: a 62-year-old man referred to our clinic due to right hand tremor associated to a slowing of idea-forming function and movements. the neuroradiological evidence showed a right fronto-tem...

Journal: :iranian journal of public health 0
adrián santana-ramirez dept. of neurosurgery, hospital civil juan i. menchaca, guadalajara, jalisco, méxico. felipe farias-serratos dept. of research, hospital regional de alta especialidad del bajío, león, guanajuato, méxico. josé sanchez-corona mexican institute of social security (imss), jalisco, centro de investigación biomédica de occidente (cibo), méxico. gema castañeda-cisneros mexican institute of social security (imss), jalisco, centro de investigación biomédica de occidente (cibo), méxico. nadia m farias-serratos dept. of surgical oncology, hospital regional de alta especialidad, cd. salud chiapas, méxico.

we report an unusual case of hemimegalencephaly (hmg) associated with ipsilateral congenital-infiltrating lipomatosis of the face in a five-month-old boy. hemimegalencephaly is a rare but unique malformation characterized by enlargement of all or parts of a cerebral hemisphere. the affected hemisphere may have focal or diffuse neuronal migration defects, with areas of polymicrogyria, pachygyria...

Journal: :iranian journal of neurology 0
alireza khoshnevisan department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. askar ghorbani department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran. narges sistany allahabadi student of medicine, school of medicine, tehran university of medical sciences, tehran, iran. farshid farzaneh department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. sina abdollahzadeh department of neurosurgery, shariati hospital, tehran university of medical sciences, tehran, iran. sepehr soleymani student of medicine, school of medicine, tehran university of medical sciences, tehran, iran.

central nervous system infection is a rare complication of endovascular procedures. we report a 21-year-old woman presented with headache, nausea, vomiting, and right-sided hemiparesis 4 months after endovascular embolization of cerebral arteriovenous malformation. investigations led to the diagnosis of multiple brain abscesses. this is the sixth case report of brain abscess following endovascu...

Journal: :bulletin of emergency and trauma 0
luis rafael moscote-salazar universidad de cartagena nasly zabaleta-churio gabriel alcala-cerra andres m. rubiano willem guillermo calderon-miranda hernando raphael alvis-miranda

chiari malformation type i (cm-i) is a congenital disorder, which is basically a tonsillar herniation (≥ 5 mm) below the foramen magnum with or without syringomyelia. the real cause behind this malformation is still unknown. patients may remain asymptomatic until they engender a deteriorating situation, such as cervical trauma. the objective of this case report is to give a broad perspective on...

Journal: :Journal of Pakistan Medical Association 2023

Dandy-Walker Malformation (DWM) is a rare congenital anomaly of the posterior cranial fossa. Features DWM include hypoplasia cerebellar vermis, enlargement fossa, and cystic dilatation fourth ventricle. MRI modality to confirm diagnosis. Treatment usually symptomatic required when signs hydrocephalus develop. Rare cases asymptomatic diagnosed incidentally are reported in literature. We report c...

Journal: :Biomedical Journal of Scientific and Technical Research 2023

Joubert syndrome (JS) is a rare autosomal dominant gene disorder that heterogeneously inherited and manifests itself as hypotonia, ataxia, breathing abnormalities, developmental delay, intellectual disabilities, oculomotor apraxia, brain malformation [1-3].

Journal: :Bali Medical Journal 2022

Spine vascular lesions like brain include spinal cord stroke, malformation such as venous or angioma, cavernous malformation, arteriovenous fistula. Embryogenesis of is the basic principle to understand spine. This study aims report serial cases with review lesions. MR angiography techniques contrast injection may reflect direction flow epidural veins describe site arterial feeders. Serpiginous...

Journal: :Malang Neurology Journal 2022

The relevance of assessing the lesion visual analyzer with optic disc drusen and possibility identifying concomitant pathologies, increases introduction latest diagnostic techniques.In S. Fyodorov Eye Microsurgery Federal State Institution, Moscow, a patient, 50 years old, complaining episodic blurred vision. diagnosis revealed nerve head congenital neurological pathology. patient was consulted...

Journal: :Neurologia I Neurochirurgia Polska 2021

The co-occurrence of a brain arteriovenous malformation, Moyamoya Disease, and intracranial aneurysm is exceedingly rare. We report the third case this disease constellation, first where arises from collateral vessel. review relevant literature discuss proposed pathophysiological mechanisms clinical implications.

2016
A. Wigan

COMMUNICATED BY THE LATE A. WIG AN, ESQ., M.D. [The history of the following case was drawn up by Dr. Wigan, a few days previously to his death during a temporary sojourn at Sussex House, Hammersmith, the residence of the Editor. More than ordinary interest will attach to the paper when it is known that it was the last professional article which this distinguished medical psychologist penned.?E...

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