Results 91 to 100 of about 4,690,855 (196)

RCC1 neuropathy mimics childhood axonal Guillain–Barré syndrome with variable clinical severity and survival

Developmental Medicine &Child Neurology, EarlyView.
We present 10 patients who presented with acute onset axonal neuropathy following infection, mimicking childhood axonal Guillain–Barré syndrome. We review phenotypes, undertake survival analysis, and assess function of novel RCC1 variants in vitro. Abstract Aim To assess the phenotype and genotype of 10 new patients with biallelic RCC1 variants who ...
Han Zhang, Beril Din, John H. McDermott, RCC1 Neuropathy Study Group, Adam Jackson, Halil Tuna Akar, Ali Dursun, Riza Koksal‐Ozgul, Reza Sadjadi, Lauren Politica, Stephan Zuchner, Reza Maroofian, Usman Ali, Dudu Turkyilmaz, Jawadur Rahman, Hasan Bas, Khalid Hussain, Khalid A Fakhro, Aljazi Al‐Maraghi, Annemarie CS Knijnenburg, Monique Engel, Debby Hellebrekers, Heike Losch, Sietse M Aukema, Marlene Kullik, Christoph Geier, Raymond T. O'Keefe, William G. Newman, J. Robert Harkness   +28 more
wiley   +1 more source

Prevalence and Disability of Peripheral Neuropathy in Patients With Waldenström's Macroglobulinemia

European Journal of Haematology, EarlyView.
ABSTRACT Objectives Peripheral neuropathy (PN) is considered a frequent complication of Waldenström's macroglobulinemia (WM). Establishing a causal relationship between PN and WM is complicated by confounding factors such as age‐related axonal loss and diabetes. This scoping review aims to summarize the current evidence on WM‐associated PN with a focus
Morten Müller Aagaard, Kristoffer Nagy Skaastrup, Louise Sloth Kodal, Britt Stævnsbo Pedersen, Troels Hammer, John Vissing, Tina Dysgaard   +6 more
wiley   +1 more source

Primary Sjögren′s syndrome manifesting as multiple cranial neuropathies: MRI findings

Annals of Indian Academy of Neurology, 2009
We report a case of primary Sjögren′s syndrome presenting with multiple cranial nerve palsies and radiological evidence of cranial pachymeningitis and hypophysitis.
Ashraf V, Bhasi Ramesh, Kumar R, Girija A   +3 more
doaj  

Standing diverticulectomy for treatment of a pulsion oesophageal diverticulum in a horse

Equine Veterinary Education, EarlyView.
Summary A 7‐year‐old Quarter Horse gelding was presented for evaluation and treatment of a pulsion oesophageal diverticulum diagnosed 8 months earlier following repeated episodes of oesophageal obstruction. Diagnostic imaging—including cervical radiographs, ultrasound and endoscopy—was used to diagnose and evaluate the lesion and guide surgical ...
Y. Tanaka, D. Major
wiley   +1 more source

Cranial nerve neuropathies: a rare manifestation of cat scratch disease

Background Cranial nerve neuropathies represent a rare manifestation of cat scratch disease (CSD). Only a few case reports have been published, and the full clinical spectrum remains poorly characterized.
Yakubovsky, Michal, Yahav, Dafna, Giladi, Michael, Gadoth, Avi, Alex Kosman, Yael Paran, Oren Zimhony, Grisaru-Soen, Galia, Avi Gadoth, Galia Grisaru-Soen, Strahilevitz, Jacob, Kadar, Laliv, Zimhony, Oren, Moshe Ephros, Kosman, Alex, Dafna Yahav, Jacob Strahilevitz, Ephros, Moshe, Michal Yakubovsky, Ronen Ben-Ami, Paran, Yael, Ben-Ami, Ronen, Michael Giladi, Laliv Kadar   +23 more
core   +1 more source

Successful rituximab treatment of granulomatosis with polyangiitis with cranial neuropathies

, 2018
Background In granulomatosis with polyangiitis (GPA), peripheral nerve involvement is common but central nervous system (CNS) involvement is extremely rare and treatment strategy has not been established. We report a case of intravenous cyclophosphamide (
Kunihiro Yamaoka, Tsutomu Takeuchi, Hidekata Yasuoka, Maho Nakazawa, Katsuya Suzuki   +4 more
core   +1 more source

A case of myeloid sarcoma presenting with an orbital mass, hearing loss, and multiple cranial neuropathies

The Turkish Journal of Pediatrics, 2018
Primary myeloid sarcoma occurring in multiple sites; orbit, ear, brain, and spinal cord is a rare clinical entity. A 15-year-old male adolescent presented with bilateral orbital mass, hearing difficulty, and clinical signs of multiple cranial nerves ...
Seon-Hee Lim, Hye-Na Nam, Kyung-In Lim, In-Sang Jeon   +3 more
doaj   +1 more source

COVID‐19–Induced Narcolepsy Type I With Cataplexy: A Short Report

Journal of Sleep Research, EarlyView.
ABSTRACT Narcolepsy type I is a rare neurological sleep disorder characterised by chronic excessive daytime sleepiness, cataplexy, and low orexin (hypocretin) levels. Infection with SARS‐CoV‐2 has been linked to neurological and neuropsychiatric sequelae, but cases of post‐COVID narcolepsy remain extremely uncommon.
Torsten Vinding Merinder, Martin Langeskov‐Christensen, Filip Kirov   +2 more
wiley   +1 more source

Ewing Sarcoma in Infants and Children Under 2 Years of Age: A French Retrospective Study

Pediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
ABSTRACT Ewing sarcoma, the second most common primary bone cancer in children, requires intensive treatment that may lead to significant long‐term sequelae, particularly in infants. We retrospectively analyzed data from 1621 French patients treated between 1988 and 2015 within the EW88/93/97 or EE99 trials, focusing on 17 infants diagnosed before 24 ...
Elodie Verdier, Nathalie Cozic, Marie‐Dominique Tabone, Gaelle Pierron, Perrine Marec‐Berard, Sarah Winter, Gabriel Revon‐Rivière, Cyril Lervat, Dominique Plantaz, Marie‐Pierre Castex, Gregory Guimard, Estelle Thebaud, Stephanie Proust, Laure Saumet, Natacha Entz‐Werle, Sophie Taque, Cécile Vérité, Marta Jimenez, Nathalie Gaspar   +18 more
wiley   +1 more source

Metachromatic Leukodystrophy Presenting with Multiple Cranial Nerve and Lumbosacral Nerve Root Enhancement Without White Matter Changes

Neurology International
Background: Metachromatic leukodystrophy (MLD) is a rare autosomal recessive disorder that causes demyelination of both the central (CNS) and peripheral nervous systems (PNS). Objective: This study aims to report a unique MLD case presenting with cranial
Ruben Jauregui, Mekka R. Garcia, Thomas Mehuron, Steven L. Galetta, Devorah Segal   +4 more
doaj   +1 more source