July 2025
A 22-year-old male, born of nonconsanguineous parentage, presented with insidious onset, gradually progressive symmetrical upper limb and lower limb ataxia, dysarthria, and distal upper and lower limb weakness since the age of eight years.
Indian Society of Neuroradiology (ISNR)
A 22-year-old male, born of nonconsanguineous parentage, presented with insidious onset, gradually progressive symmetrical upper limb and lower limb ataxia, dysarthria, and distal upper and lower limb weakness since the age of eight years.
20 year old male patient presented with headache for 2 days, altered sensorium and single episode of seizure. He had a major road traffic accident one week back.
An 11-year-old female presented with complaints of progressive weakness of the left upper and lower limbs for 1 year, dysphagia for 4 months, reduced vision in the left eye for 3 months, dysarthria for 2 months, and urinary incontinence for 15 days.
A 16-year-old male presented with short stature, bilateral ptosis, diplopia, and Type 1 diabetes mellitus. Family history is significant for short stature and ptosis.
35 years old lady with abnormal antenatal ultrasound came for fetal MRI at 33 weeks of gestation.
A 11-year-old male child presented with long-standing drug-resistant epilepsy. NCCT head was performed after a seizure episode in the neuro casualty, subsequently MRI brain was performed for further characterization.
A rare case of osmotic pontine demyelination due to hypokalemia in a patient with Sjogren syndrome and renal tubular acidosis.
9 years old child presented to pediatrics emergency with cyanotic spell and headache. He was a known case of tetralogy of Fallot with a large VSD. On examination – the child had peripheral and central cyanosis.
39 years , male, presented with progressive gait disturbance and speech difficulty since 11 months. Associated with headache, giddiness and vomiting since 3-4 months.
A 31 year old male presented with history of seizures since 2 months. He was treated with anti epileptics and was well controlled. Patient again developed breakthrough seizures. No focal neurological deficits. Auto immune work up & CSF analysis were unremarkable.