keyword
https://read.qxmd.com/read/38537312/small-fiber-neuropathy-in-children-adolescents-and-young-adults-with-chronic-orthostatic-intolerance-and-postural-orthostatic-tachycardia-syndrome-a-retrospective-study
#21
JOURNAL ARTICLE
Jeffrey P Moak, Carolyn B Ramwell, Heather Gordish-Dressman, Sangeeta D Sule, Elizabeth Bettini
PURPOSE: To determine in children, adolescent and young adult (CAYA) patients presenting with Orthostatic Intolerance (OI) or Postural Orthostatic Tachycardia Syndrome (POTS) associated with the additional symptoms of neuropathic discomfort (pain, paresthesia and/or allodynia): 1) the incidence of small fiber neuropathy, and 2) assess if there was serologic evidence for an underlying inflammatory or autoimmune state. METHODS: A cohort of 109 CAYA patients with the above symptoms underwent epidermal skin biopsy for nerve fiber density...
March 8, 2024: Autonomic Neuroscience: Basic & Clinical
https://read.qxmd.com/read/38534782/clinical-genomic-analysis-of-1261-patients-with-ehlers-danlos-syndrome-outlines-an-articulo-autonomic-gene-network-entome
#22
JOURNAL ARTICLE
Golder N Wilson, Vijay S Tonk
Systematic evaluation of 80 history and 40 history findings diagnosed 1261 patients with Ehlers-Danlos syndrome (EDS) by direct or online interaction, and 60 key findings were selected for their relation to clinical mechanisms and/or management. Genomic testing results in 566 of these patients supported EDS relevance by their differences from those in 82 developmental disability patients and by their association with general rather than type-specific EDS findings. The 437 nuclear and 79 mitochondrial DNA changes included 71 impacting joint matrix (49 COL5 ), 39 bone (30 COL1/2/9/11 ), 22 vessel (12 COL3/8VWF) , 43 vessel-heart (17 FBN1 /11 TGFB / BR) , 59 muscle (28 COL6/12 ), 56 neural (16 SCN9A / 10A / 11A ), and 74 autonomic (13 POLG /25porphyria related)...
March 19, 2024: Current Issues in Molecular Biology
https://read.qxmd.com/read/38529548/exploring-multiple-endocrinological-issues-and-dysautonomia-in-a-rare-case-hypoparathyroidism-in-mirage-syndrome
#23
JOURNAL ARTICLE
Sirmen Kızılcan Çetin, Elif Özsu, Zeynep Şıklar, Hasan Fatih Çakmaklı, Gizem Şenyazar, Zehra Aycan, Serdar Ceylaner, Merih Berberoğlu
MIRAGE syndrome is a rare multisystemic disorder characterized by various manifestations, such as myelodysplasia, susceptibility to infections, growth retardation, adrenal hypoplasia, genital anomalies, and enteropathy. In the literature, there have been rare cases of dysautonomia. We present a 6.5-year-old girl, who was first admitted to our department with short stature. On follow up, she exhibited multiple endocrinological issues, including transient hypothyroidism, primary hypoparathyroidism and dysautonomia, along with multisystem involvement...
March 26, 2024: Journal of Clinical Research in Pediatric Endocrinology
https://read.qxmd.com/read/38526146/complete-remission-with-histamine-blocker-in-a-patient-with-intractable-hyperadrenergic-postural-orthostatic-tachycardia-syndrome-secondary-to-long-coronavirus-disease-syndrome
#24
JOURNAL ARTICLE
Felipe González-Alvarez, Bruno Estañol, Jesús Antonio González-Hermosillo, Francisco Javier Gómez-Pérez, Karla Maria Tamez-Torres, Eduardo Peña, Carlos Cantú, Erwin Chiquete, José Sifuentes-Osornio, Maria Del Carmen Alba-Lorenzo, Dulce Andrea Celestino-Montelongo, Guadalupe E Salazar-Calderón, Jose de Jesus Aceves Buendia
The COVID-19 pandemic caused by the novel severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), has emerged as a global public health concern and its sequels have barely started to outcrop. A good percentage of patients who suffered from COVID-19 are prone to develop long-COVID or post-COVID condition (PCC), a multisystemic, heterogeneous, chronic disorder. Patients with PCC may experience diverse manifestations, of which cardiovascular and neurological symptoms are among the most frequently reported...
March 11, 2024: Journal of Hypertension
https://read.qxmd.com/read/38512841/web-based-survey-investigating-cardiovascular-complications-in-hypermobile-ehlers-danlos-syndrome-after-covid-19-infection-and-vaccination
#25
JOURNAL ARTICLE
Anthony L Guerrerio, Allyson Mateja, Gretchen MacCarrick, Jonathan Fintzi, Erica Brittain, Pamela A Frischmeyer-Guerrerio, Harry C Dietz
BACKGROUND: Hypermobile Ehlers-Danlos syndrome is a heritable connective tissue disorder associated with generalized joint hypermobility but also other multisystem comorbidities, many of which may be exacerbated during a viral illness or after a vaccination. We sought to determine whether individuals with hypermobile Ehlers Danlos syndrome report an increase in adverse events, including cardiovascular events, after COVID-19 illness or vaccination. METHODS: A cross-sectional web-based survey was made available from November 22, 2021, through March 15, 2022...
2024: PloS One
https://read.qxmd.com/read/38511726/correction-to-exon-specific-u1-snrnas-improve-elp1-exon-20-definition-and-rescue-elp1-protein-expression-in-a-familial-dysautonomia-mouse-model
#26
(no author information available yet)
No abstract text is available yet for this article.
March 21, 2024: Human Molecular Genetics
https://read.qxmd.com/read/38510253/case-report-rapid-recovery-after-intrathecal-rituximab-administration-in-refractory-anti-nmda-receptor-encephalitis-report-of-two-cases
#27
Mahasen Reda, Rosette Jabbour, Asad Haydar, Fatima Jaafar, Nabil El Ayoubi, Omar Nawfal, Ahmad Beydoun
BACKGROUND: Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is one of the most prevalent etiologies of autoimmune encephalitis. Approximately 25% of anti-NMDAR encephalitis cases prove refractory to both first- and second-line treatments, posing a therapeutic dilemma due to the scarcity of evidence-based data for informed decision-making. Intravenous rituximab is commonly administered as a second-line agent; however, the efficacy of its intrathecal administration has rarely been reported...
2024: Frontiers in Immunology
https://read.qxmd.com/read/38501557/significance-of-dysautonomia-in-parkinson-s-disease-and-atypical-parkinsonisms
#28
JOURNAL ARTICLE
Piotr Alster, Natalia Madetko-Alster
No abstract text is available yet for this article.
March 19, 2024: Neurologia i Neurochirurgia Polska
https://read.qxmd.com/read/38499084/beyond-confirmed-mast-cell-activation-syndrome-approaching-patients-with-dysautonomia-and-related-conditions
#29
REVIEW
Alexandra E Conway, Marylee Verdi, Marcus S Shaker, Jonathan A Bernstein, Claire C Beamish, Richard Morse, Juliette Madan, Michael W Lee, Gordon Sussman, Amer Al-Nimr, Matthew Hand, Daniel A Albert
Allergist-immunologists face significant challenges as experts in an ever-evolving field of neuroimmunology. Among these challenges is the increasingly frequent need to counsel patients with suspected mast cell-activation disorders about perceived comorbidities, which may include hypermobile Ehlers Danlos syndrome, amplified pain syndrome, fibromyalgia, burning sensation syndromes, migraines, irritable bowel syndrome, and postural orthostatic tachycardia syndrome. Patients may experience comorbid anxiety, panic disorder and depression associated with disturbed sleep, fatigue, and cognitive impairment that often worsen when their physical symptoms increase in severity...
March 16, 2024: Journal of Allergy and Clinical Immunology in Practice
https://read.qxmd.com/read/38494470/dysautonomia-in-anti-hu-paraneoplastic-neurological-syndromes
#30
JOURNAL ARTICLE
Macarena Villagrán-García, Antonio Farina, Joaquín Arzalluz-Luque, Lucia Campetella, Sergio Muñiz-Castrillo, Marie Benaiteau, Elise Peter, Pauline Dumez, Valentin Wucher, Maroua Dhairi, Géraldine Picard, Marie Rafiq, Dimitri Psimaras, Véronique Rogemond, Bastien Joubert, Jérôme Honnorat
BACKGROUND AND OBJECTIVES: Dysautonomia has been associated with paraneoplastic neurological syndrome (PNS)-related mortality in anti-Hu PNS, but its frequency and spectrum remain ill-defined. We describe anti-Hu patients with dysautonomia, estimate its frequency, and compare them to patients without dysautonomia. METHODS: Patients with anti-Hu antibodies diagnosed in the study centre (1990-2022) were retrospectively reviewed; those with autonomic signs and symptoms were identified...
March 17, 2024: Journal of Neurology
https://read.qxmd.com/read/38494291/paraneoplastic-autoimmune-neurologic-disorders-associated-with-thymoma
#31
REVIEW
Raffaele Iorio, Vanda A Lennon
Thymoma is often associated with paraneoplastic neurologic diseases. Neural autoantibody testing is an important tool aiding diagnosis of thymoma and its autoimmune neurologic complications. Autoantibodies specific for muscle striational antigens and ion channels of the ligand-gated nicotinic acetylcholine receptor superfamily are the most prevalent biomarkers. The autoimmune neurologic disorders associating most commonly with thymoma are myasthenia gravis (MG), peripheral nerve hyperexcitability (neuromyotonia and Morvan syndrome), dysautonomia, and encephalitis...
2024: Handbook of Clinical Neurology
https://read.qxmd.com/read/38489192/characterizing-heart-rate-variability-response-to-maximal-exercise-testing-in-people-with-huntington-s-disease
#32
JOURNAL ARTICLE
Haoyu Li, Radhika Desai, Norberto Quiles, Lori Quinn, Ciarán Friel
BACKGROUND: Huntington's disease (HD) is an autosomal dominant, neurodegenerative disease that involves dysfunction in the autonomic nervous system (ANS). Heart rate variability (HRV) is a valid and noninvasive measure for ANS dysfunction, yet no study has characterized HRV response to exercise in people with HD. OBJECTIVE: Characterize HRV response to exercise in individuals with HD and explore its implications for exercise prescription and cardiac dysautonomia mechanisms...
March 14, 2024: Journal of Huntington's Disease
https://read.qxmd.com/read/38487322/isolated-insular-stroke-topography-is-the-answer-with-respect-to-outcome-and-cardiac-involvement
#33
JOURNAL ARTICLE
Fedra Kuris, Sara Tartaglia, Roberto Sperotto, Laura Ceccarelli, Daniele Bagatto, Simone Lorenzut, Giovanni Merlino, Francesco Janes, Carolina Gentile, Roberto Marinig, Lorenzo Verriello, Mariarosaria Valente, Giada Pauletto
BACKGROUND AND PURPOSE: Isolated insular strokes (IIS) are a rare occurrence due to the frequent concomitant involvement of adjacent territories, supplied by the M2 segment of the middle cerebral artery (MCA), and clinical aspects are sometimes contradictory. We aimed to describe clinical and radiological characteristics of a pure IIS case series, focusing on its functional outcome and cardiac involvement. METHODS: We identified 15 isolated insular ischemic strokes from a pool of 563 ischemic strokes occurred between January 2020 and December 2021...
2024: Frontiers in Neurology
https://read.qxmd.com/read/38466015/neurological-autoimmunity-in-patients-with-non-pulmonary-neuroendocrine-neoplasms-clinical-manifestations-and-neural-autoantibody-profiles
#34
JOURNAL ARTICLE
Georgios Mangioris, Thorvardur R Halfdanarson, Vanda A Lennon, Bryce K Chang, Divyanshu Dubey, P James B Dyck, Eoin P Flanagan, Andrew McKeon, John R Mills, Sean J Pittock, Anastasia Zekeridou
BACKGROUND AND PURPOSE: Paraneoplastic neurological autoimmunity is well described with small-cell lung cancer, but information is limited for other neuroendocrine neoplasms (NENs). METHODS: Adult patients with histopathologically confirmed non-pulmonary NENs, neurological autoimmunity within 5 years of NEN diagnosis, and neural antibody testing performed at the Mayo Clinic Neuroimmunology Laboratory (January 2008 to March 2023) were retrospectively identified...
March 11, 2024: European Journal of Neurology
https://read.qxmd.com/read/38464711/evaluation-of-the-existence-of-post-covid-19-tachycardia-in-a-community-healthcare-system
#35
JOURNAL ARTICLE
Jifeng Wang, Dhaval Patel, Shane Robinson, Ania Rynarzewska, Oluseyi Abidoye
BACKGROUND: Post-coronavirus disease 2019 (COVID-19) syndrome derives from lingering symptoms after an acute COVID-19 infection. Palpitation was one of the most common symptoms of post-COVID-19 syndrome that correlated with objective data such as persisting sinus tachycardia; but to our best knowledge, there is a scarcity of research regarding the association of COVID-19 and sinus tachycardia in the post-acute setting. Therefore, the purpose was to identify if there is an association between COVID-19 infection and sinus tachycardia in the post-acute phase, namely post-COVID-19 tachycardia (PCT) other than inappropriate sinus tachycardia (IST) and postural orthostatic tachycardia syndrome (POTS)...
February 2024: Cardiology Research
https://read.qxmd.com/read/38458016/an-open-trial-of-biofeedback-for-long-covid
#36
JOURNAL ARTICLE
Natacha D Emerson, Helen Lavretsky, William Q Pittman, Nisha Viswanathan, Prabha Siddarth
OBJECTIVE: Biofeedback is a therapeutic treatment model that teaches self-regulation of autonomic functions to alleviate stress-related symptoms. "Long COVID" refers to chronic physical and cognitive sequelae post-SARS-CoV-2 infection. This study examined the efficacy of a six-week intervention, consisting of weekly one-hour sessions combining heart rate variability and temperature biofeedback, for alleviating mood symptoms, somatic symptoms and sleep disturbance of patients diagnosed with long COVID...
February 23, 2024: Journal of Psychosomatic Research
https://read.qxmd.com/read/38456315/prevalence-of-orthostatic-intolerance-in-long-covid-clinic-patients-and-healthy-volunteers-a-multicenter-study
#37
MULTICENTER STUDY
Cassie Lee, Darren C Greenwood, Harsha Master, Kumaran Balasundaram, Paul Williams, Janet T Scott, Conor Wood, Rowena Cooper, Julie L Darbyshire, Ana Espinosa Gonzalez, Helen E Davies, Thomas Osborne, Joanna Corrado, Nafi Iftekhar, Natalie Rogers, Brendan Delaney, Trish Greenhalgh, Manoj Sivan
Orthostatic intolerance (OI), including postural orthostatic tachycardia syndrome (PoTS) and orthostatic hypotension (OH), are often reported in long covid, but published studies are small with inconsistent results. We sought to estimate the prevalence of objective OI in patients attending long covid clinics and healthy volunteers and associations with OI symptoms and comorbidities. Participants with a diagnosis of long covid were recruited from eight UK long covid clinics, and healthy volunteers from general population...
March 2024: Journal of Medical Virology
https://read.qxmd.com/read/38441929/anti-plexin-d1-seropositive-small-fiber-neuropathy-clinical-phenotype-demographics-and-literature-review
#38
REVIEW
Peyton J Murin, Ivana Massabki, Jafar Kafaie
OBJECTIVES: Small fiber neuropathy (SFN) is a subtype of painful neuropathies defined by dysfunction of the Aδ and unmyelinated C fibers. It presents with both neuropathic pain and dysautonomia symptoms, posing a significant diagnostic and therapeutic challenge. To address this challenge, research has been conducted to identify autoantibodies and define their association with phenotypes. METHODS: Eleven cases of anti-plexin-D1 seropositive SFN were reviewed, along with relevant literature, in attempt to better define anti-plexin-D1 SFN demographics, symptoms, associated medical conditions, and therapeutics...
March 1, 2024: Journal of Clinical Neuromuscular Disease
https://read.qxmd.com/read/38441114/autoimmune-and-inflammatory-neurological-disorders-in-the-intensive-care-unit
#39
REVIEW
Camille Legouy, Anna Cervantes, Romain Sonneville, Kiran T Thakur
PURPOSE OF REVIEW: The present review summarizes the diagnostic approach to autoimmune encephalitis (AE) in the intensive care unit (ICU) and provides practical guidance on therapeutic management. RECENT FINDINGS: Autoimmune encephalitis represents a group of immune-mediated brain diseases associated with antibodies that are pathogenic against central nervous system proteins. Recent findings suggests that the diagnosis of AE requires a multidisciplinary approach including appropriate recognition of common clinical syndromes, brain imaging and electroencephalography to confirm focal pathology, and cerebrospinal fluid and serum tests to rule out common brain infections, and to detect autoantibodies...
April 1, 2024: Current Opinion in Critical Care
https://read.qxmd.com/read/38425333/complex-dysautonomia-in-a-patient-with-cerebral-cavernous-malformations-due-to-a-krit1-pleiotropic-gene-mutation
#40
Roel Janssen, Maxime Ariëns, Jessie van Genugten, Linda Jacobi, Ger Koek
Dysautonomia is a disruption of the body's autonomic processes. Symptoms vary among patients, depending on the underlying disease pathways. Given that symptoms can affect all organ functions, dysautonomia often significantly impacts quality of life. However, due to its complex and varied presentation, early recognition of dysautonomia remains a challenge, yet it is crucial for improving patient outcomes. We report a case of a patient with a KRIT1 mutation presenting with dysautonomia causing urological, sexual, and bowel dysfunction...
February 2024: Curēus
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