Results 51 to 60 of about 4,366 (203)

Behavioral Phenotype and Neuropsychological Profile of an Adult With Smith‐Magenis Syndrome due to a Previously Unreported RAI1 Mutation: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Smith‐Magenis Syndrome (SMS) is an uncommon genetic disorder caused by microdeletions of chromosome 17p11.2 including the RAI1 gene, or loss‐of‐function mutations that directly affect RAI1. Due to the involvement of RAI1 in neurodevelopment, SMS leads to typical pathologic features in the behavioral and physical phenotype that must be ...
Edgar Andrés Chavarría‐Martínez, Julen Arellano‐Sandúa, Ruth Arias‐Hidalgo, Ana Patiño‐García, Adrián Cano‐Prous   +4 more
wiley   +1 more source

Pseudotumor Cerebri and Sickle Cell Disease

Pediatric Neurology Briefs, 2004
Three children, all girls, ages 9, 8, and 16 years, with sickle cell disease (SCD) presented with headache and were diagnosed with pseudotumor cerebri (PC) at the Children’s National Medical Center, Washington, DC.
J Gordon Millichap
doaj   +1 more source

Fibrinolysis in Pseudotumor Cerebri

Annals of Saudi Medicine, 1993
Pseudotumor cerebri is a syndrome associated with diverse putative etiological factors that include chemicals such as vitamin A, tetracycline and estrogens or venous circulatory disturbances like sagittal or transverse sinus thrombosis. Diseases predisposing to thrombosis, such as polycythemia vera and essential thrombocythemia, were reported to cause ...
M Z, Al-Kawi, P S, Chavis, G T, Roberts
openaire   +2 more sources

Inflammation in Idiopathic Intracranial Hypertension: An Immunometabolic Mechanistic Framework and Clinical Implications

CNS Neuroscience &Therapeutics, Volume 32, Issue 3, March 2026.
Systemic metabolic dysfunction and comorbidities may act as upstream modulators converging on inflammatory activation, which is closely intertwined with excessive CSF production and impaired clearance, potentially contributing to sustained ICP elevation.
Guangyu Han, Jiahao Song, Shuling Wan, Xunming Ji, Da Zhou, Ran Meng   +5 more
wiley   +1 more source

Pseudotumor cerebri and Chiari Malformation [PDF]

, 2015
Power point of case presentation of pseudotumor cerebri with co-existing Chiari malformation. Management of severe visual loss associated with chronic papilledema discussed, as well as possible relationship between raised intracranial pressure from ...
Nicole Scripsema, MD; Rudrani Banik, MD
core  

Surgical Interventions in Idiopathic Intracranial Hypertension—A Comprehensive Multi‐Center Study of Outcome and the Role of Treatment Indication

European Journal of Neurology, Volume 33, Issue 3, March 2026.
In this multicenter retrospective study of idiopathic intracranial hypertension, only 3.6% of patients required surgery, predominantly for acute visual deterioration. Both cerebrospinal fluid diversion and optic nerve sheath fenestration were effective in improving visual outcomes and resolving papilledema, while headache improvement was limited ...
Gabriel Bsteh, Nadja Skadkær Hansen, Sina Zaic, Steffen Hamann, Johanne Juhl Korsbæk, Nik Krajnc, Stefan Macher, Laleh Dehghani Molander, Klaus Novak, Therese Wallentin Steenfos, Marianne Wegener, Berthold Pemp, Rigmor Højland Jensen, Dagmar Beier, Kaare Fugleholm, Marianne Juhler, Karl Kirchner, Martin Michl, Christoph Mitsch, Nina Müller, Petersen Bibi Gronemann, Andreas Reitner, Christoph Stapf, Christian Wöber, Karin Zebenholzer   +24 more
wiley   +1 more source

Miller Fisher Syndrome Presenting as Pseudotumor

Pediatric Neurology Briefs, 2002
Two female children, ages 9 and 2 years, who presented with pseudotumor cerebri and within 2 to 3 days, were diagnosed with Miller Fisher syndrome are reported from the Hopital Universitaire des Enfants Reine Fabiola, Brussels, Belgium.
J Gordon Millichap
doaj   +1 more source

Idiopathic Intracranial Hypertension—Clinical Characteristics, Neuroimaging and Outcome of Patients from Pretoria, South Africa

Neurology and Clinical Neuroscience, Volume 14, Issue 1, Page 46-53, January 2026.
ABSTRACT Background Idiopathic intracranial hypertension is a syndrome characterized by symptoms and signs of raised intracranial pressure without a secondary cause. It primarily affects young obese women who present with headache and papilledema. We report the clinical presentation, brain imaging findings and outcomes of patients with IIH from two ...
Bandlakazi Sukwana‐Ncemane, Juliane Hiesgen, Clara M. Schutte   +2 more
wiley   +1 more source

"Malignant" Pediatric Pseudotumor Cerebri [PDF]

, 2003
Thirty of our pediatric pseudotumor cerebri patients were evaluated to determine those at high risk for visual ...
Thomas C. Spoor, MD
core  

The Use of Combined Fundus Photography and Perimetry for the Assessment of Patients Referred for Intracranial Hypertension or Follow‐Up of the Diagnosis in a Tertiary Headache Center

European Journal of Neurology, Volume 33, Issue 1, January 2026.
ABSTRACT Objectives Idiopathic intracranial hypertension (IIH) is characterized by increased intracranial pressure and papilledema. If left untreated, it can lead to vision loss, and, timely detection of papilledema is of paramount importance. Direct ophthalmoscopy can be difficult to perform and interpret for non‐ophthalmologists.
Zainab Rissan, Nadja Skadkær Hansen, Vlasta Vukovic‐Cvetkovic, Louise Ninett Carlsen, Steffen Hamann, Marianne Wegener, Rigmor H. Jensen, Henrik Winther Schytz   +7 more
wiley   +1 more source