A5075779998- Long-Term Effects of COVID-19
- Infectious Encephalopathies and Encephalitis
- Meningioma and schwannoma management
- Cerebrospinal fluid and hydrocephalus
- Intracranial Aneurysms: Treatment and Complications
- Vascular Malformations Diagnosis and Treatment
- Head and Neck Surgical Oncology
- Infectious Diseases and Tuberculosis
- Metabolism and Genetic Disorders
- Peripheral Neuropathies and Disorders
- Sinusitis and nasal conditions
- Hearing, Cochlea, Tinnitus, Genetics
- Neurosurgical Procedures and Complications
- Antifungal resistance and susceptibility
- Genetic and rare skin diseases.
- Intracerebral and Subarachnoid Hemorrhage Research
- Cerebral Venous Sinus Thrombosis
- Spinal Dysraphism and Malformations
- Neurological and metabolic disorders
- RNA regulation and disease
- Brain Metastases and Treatment
- Autoimmune Neurological Disorders and Treatments
- Neurological diseases and metabolism
- Hearing Loss and Rehabilitation
- Glioma Diagnosis and Treatment
All India Institute of Medical Sciences Jodhpur
2019-2025
All India Institute of Medical Sciences
1998-2024
Creative Commons
2023
Institute of Neurosciences Kolkata
2019-2020
Institut des Maladies Génétiques Imagine
2020
Royal Victoria Infirmary
2020
Institute of Genetics and Cancer
2020
University of Edinburgh
2020
The Neurosciences Foundation
2020
Manchester Academic Health Science Centre
2020
Neurologic manifestation of coronavirus disease 2019 (COVID-19) in children is evolving with time. We are reporting a young girl who presented to us acute febrile illness followed by onset severe flaccid paralysis requiring prolonged intensive care unit stay and ventilator support. She was evaluated extensively found be positive for COVID serology, neuroimaging revealed features longitudinally extensive transverse myelitis (LETM) enhancing cauda equina nerve roots, suggesting Guillain-Barré...
A 14-year-old developmentally normal boy who was otherwise healthy presented with progressive stiffness involving the face, trunk, and all four limbs. His illness started 25 days back when he developed fever, projectile vomiting, headache, which were relieved symptomatic management. Two weeks later, child emotional lability restricted movements of limbs progressing to generalized movement restriction in next 5 days. There no history recent travel, vaccination, drug intake, or any high-risk...
Abstract Introduction: Hansen’s disease is a chronic, infective granulomatous skin with wide array of manifestations that resemble many dermatological and neurological conditions. Pure neuritic familiar form among leprosy physicians, it poses significant diagnostic difficulty. Various disorders can mimic neuropathy clinically these patients may receive multidrug therapy in endemic areas due to the commonality leprosy. Hence, necessary be aware mimickers its various forms. Patients Methods:...
To assess the relation between cochlear duct length (CDL) and audiological outcome after implant surgery in prelingually deafened children. In a prospective cohort study, 36 deaf children underwent implantation at All India Institute of Medical Sciences, Jodhpur. Preoperative high-resolution computed tomography (HRCT) T2 weighted sequences magnetic resonance imaging (MRI) temporal bones were used to calculate CDL. Patients followed up for 12 months postoperatively with visits every three...
Women of reproductive age with Von Willebrand disease (VWD) are at increased risk haemorrhagic ovarian cysts due to excessive bleeding into the corpus luteum during ovulation. The rupture these can lead life-threatening hematoperitoneum and other complications such as pelvic adhesions, fallopian tube blockages, damage, which may impair fertility. Early diagnosis management VWD critical mitigating risks. A 20-year-old unmarried woman presented emergency department acute abdominal pain...
Introduction Heimler syndrome 1 is a group of peroxisomal biogenesis disorders due to the pathogenic variations in factor ( PEX1 ) gene resulting dysfunction intracellular peroxisomes. encodes proteins that are involved import matrix proteins. Patients A 6-year-old boy, second born nonconsanguineous parents, presented with global developmental delay, progressive hearing loss, and night blindness. He had an uneventful antenatal perinatal period. significant family history similar complaints...
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) (MIM 600142) is linked to homozygous mutations in the high-temperature requirement A serine peptidase 1 gene ( HTRA1 ).1 The triad includes alopecia, spondylosis deformans, young-adult onset dementia following leukoaraiosis caused by cerebral small-vessel disease (CSVD).2 Although CARASIL originally was considered be a disorder monoethnic, restricted Japan, there are several reports of...
Abstract Background Primary central nervous system melanoma is an extremely rare entity and even rarer in children adolescents as compared to adults. It often difficult consider a diagnosis of intracranial pre-operatively without any clinical evidence neurocutaneous melanosis. Case presentation Herein, case primary the brain reported 17-year-old female who presented with headache, vomiting, focal neurological deficit form left-sided facial palsy limb weakness. A contrast-enhanced computed...
OBJECTIVE Different techniques of performing image-guided neurosurgery exist, namely, neuronavigation systems, intraoperative ultrasound, and MRI, each with its limitations. Except for other methods are expensive. Three-dimensional virtual reconstruction surgical simulation using 3D volume rendering (VR) is an economical excellent technique preoperative planning neurosurgery. In this article, the authors discuss several nuances VR that have not yet been described. METHODS The included 6...
Fibro adipose vascular anomaly (FAVA) is a rare type of malformation with distinct clinical features. The authors here discussed the clinical, imaging, differential diagnosis, histopathological features, and treatment options FAVA along an illustrative case. It important to know about this uncommon entity as can be misdiagnosed due overlapping features other common entities. benign condition no proven malignant potential. There are guidelines regarding best option.