WalidoNeuroPedia

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WalidoNeuroPedia

WalidoNeuroPedia

@NeuroWalid

Empowering Neuro Education: Tips, research updates & book recommendations for Neuro residents, students & specialists. Unlocking brain mysteries! 🧠🔔#Neurotip

Canada Присоединился Nisan 2024
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WalidoNeuroPedia
WalidoNeuroPedia@NeuroWalid·
Gelastic seizures, marked by bouts of uncontrollable laughter, are classically linked to hypothalamic hamartomas. They may also be associated with Pallister-Hall syndrome (caused by a GLI3 mutation on chromosome 7). Present in infancy. EEG often normal due to deep seizure focus. #neurotip #neuropediatrics #epilepsy
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WalidoNeuroPedia
WalidoNeuroPedia@NeuroWalid·
An easy way to differentiate these midbrain syndromes is to remember that, moving from anterior to posterior, all three involve oculomotor nerve damage, with additional distinct features: Weber’s syndrome – affects the anterior midbrain, involving the corticospinal tracts, leading to contralateral weakness. Benedikt’s syndrome – involves the mid-midbrain, including the red nucleus, causing abnormal involuntary movements such as tremor and chorea. Claude’s syndrome – localized to the posterior midbrain, where superior cerebellar peduncle fibers (after decussation) are affected, resulting in cerebellar signs (think Claude = Cerebellar). #Neurotip
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NEUROMAN DR.
NEUROMAN DR.@DrADAM34927388·
@NeuroWalid And never foget Nothnagel's syndrome involving the dorsal (tectum) midbrain >>> Ipsilateral 3rd palsy + Ipsilateral cerebellar ataxia ( the opposite fo Claude's)!!!
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Mário@BuckBanzai08·
@NeuroWalid Consider not if CAA… dubious phrasing. You would not consider if CAA or if prior hemorrhagic stroke?
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د. محمد الشمري
د. محمد الشمري@MohdNeuro·
@NeuroWalid This is outdated, especially after multiple trials and the CATALYST meta analysis, which supports early (less than or equal 4 days) in ischemic strokes.
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WalidoNeuroPedia
WalidoNeuroPedia@NeuroWalid·
Diagnostic criteria for hereditary hemorrhagic telangiectasias: #neurotip
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WalidoNeuroPedia
WalidoNeuroPedia@NeuroWalid·
🧠 #CARASIL = Cerebral autosomal recessive arteriopathy w/ subcortical infarcts & leukoencephalopathy (HTRA1 gene). 💇‍♂️ Early-onset strokes + alopecia + spondylosis. Neuro: stepwise decline → dementia, spastic gait, mood changes. MRI: WM hyperintensities + lacunes (BG/thalamus), ± microbleeds. #neurotip #stroke
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