Results 31 to 40 of about 906,055 (304)

CASE REPORT OF ADULT-ONSET CHARCOT MARIE TOOTH TYPE X

Malang Neurology Journal, 2022
Charcot-Marie-Tooth (CMT) or Hereditary Motor and Sensory Neuropathy (HMSN) is the most common hereditary peripheral nerve disease with progressive chronic weakness, muscle atrophy, and sensory disturbances.
Richard Suherlim, Anak Agung Ayu Putri Laksmidewi, Sudiarini NKA   +2 more
doaj   +1 more source

Adult-Onset Immunoglobulin A Vasculitis

ACG Case Reports Journal, 2020
ABSTRACT Immunoglobulin A vasculitis (IgAV), formerly Henoch–Schönlein purpura vasculitis, is a vasculitis commonly seen in children and only rarely described in adult patients. IgAV can present as arthralgia, rash, discolored urine, acute kidney injury, and gastrointestinal symptoms.
Chadwick, Matthew, Shamban, Leonid, Macksood, John   +2 more
openaire   +2 more sources

Adult Onset Sacrococcygeal Teratoma

Cureus, 2023
Sacrococcygeal teratoma (SCT), one of the most common neoplastic tumors in newborns, is found very rarely in adults. These teratomas are germ cell tumours. Most of these tumors are benign and cystic in nature, with only 1-2% of them having a malignant transformation.
Baikady, Shathak S, Singaram, Nagesh K
openaire   +2 more sources

Health‐Related Quality of Life and Symptom Severity Among Patients With PIK3CA‐Related Overgrowth Spectrum: A Mixed‐Methods Study to Understand Real‐World Experience With Alpelisib Treatment

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background PIK3CA‐related overgrowth spectrum (PROS) includes several rare overgrowth disorders resulting from somatic gain‐of‐function mutations in PIK3CA. Despite treatment advances, including the recent approval of alpelisib for PROS in the United States, literature detailing the patient experience with PROS is limited.
Vamsi Bollu, Kaitlin LaGasse, Cory D. Saucier, Kimberly Raymond, Miranda Lauher‐Charest, Lauren Crowder, Beilei Cai, Mary Lisha Paul, Denise Adams   +8 more
wiley   +1 more source

Venous Thromboembolism in Pediatric Bone Sarcoma Patients: A 10‐Year, Single‐Institution Experience Encompassing the COVID‐19 Pandemic

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Osteosarcoma (OS) and Ewing sarcoma (EWS) are the most common primary bone cancers in children, but acute thrombosis is poorly characterized in this population. Our study evaluated the rates of venous thromboembolism (VTE) and associated risk factors in pediatric patients with bone sarcomas treated over a 10‐year period encompassing
Sarah Kappa, Shou Xu, Mark Zobeck, Sarah E. Sartain, Nino Rainusso, Lisa Wang, Nicole Montgomery, Paige Wheaton, Sarah Whittle   +8 more
wiley   +1 more source

Adult‐Onset Still's Disease(AOSD) With Features Suggestive of Macrophages Activation Syndrome in Young Female: A Rare Case Report From Nepal

Clinical Case Reports
Adult‐onset Still's disease (AOSD) is a rare, multisystem autoinflammatory disorder characterized by a classic triad of fever, evanescent rash, and arthritis with diagnostic challenges.
Sushil Silwal, Krishan Khang Mandal, Gaurav Parajuli, Krishna Adhikari   +3 more
doaj   +1 more source

Adult-onset erythrokeratodermia variabilis (EKV) triggered by pregnancy and crash dieting: A rare case report

Journal of the Pakistan Medical Association
Erythrokeratodermia variabilis (EKV) is a rare inherited genodermatosis characterised by migratory and erythematous patches changing over the course of hours to days and fixed keratotic plaques.
Ghazal Afzal, Najia Ahmed, Nighat Jamal, Fatima Zahoor   +3 more
doaj   +1 more source

Emapalumab for Immune Effector Cell‐Associated Hemophagocytic Lymphohistiocytosis‐Like Syndrome Following CD19‐Directed CAR‐T in Two Patients With B‐ALL: Clinical and Biomarker Correlates

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Immune effector cell‐associated hemophagocytic lymphohistiocytosis‐like syndrome (IEC‐HS) is a life‐threatening hyperinflammatory toxicity distinct from cytokine release syndrome (CRS) and neurotoxicity following chimeric antigen receptor T‐cell (CAR‐T) therapy. In a single‐institution retrospective cohort of pediatric and young adult patients
Thomas J. Galletta, Jeremy D. Rubinstein, Christopher E. Dandoy, Ruby Khoury, Angela Faulhaber, Christine L. Phillips, Christa Krupski   +6 more
wiley   +1 more source

Elderly-onset adult Still’s disease

Rheumatology, 2021
Adult-onset Still’s disease is a rare inflammatory disorder usually affecting young adults. Elderly-onset Still’s disease (EOSD) is reported in some cases, commonly in Japan, the USA and Europe.
Anis Mzabi, Rym Fakhfakh, Maissa Thabet, Imen Ben Hassine, Jihed Anoun, Monia Karmani, Fatma Ben Fredj, Chadia Laouani   +7 more
doaj   +1 more source

Lower limb involvement in adult-onset primary dystonia: frequency and clinical features

, 2010
Despite the growing number of reports describing adult-onset primary lower limb dystonia (LLD) this entity has never been systematically evaluated in the general population of patients with primary adult-onset ...
Liuzzi, D., GIRLANDA P, Fabbrini G., LIGUORI, ROCCO, Girlanda, P., SABETTA A, Guidubaldi, Arianna, MORGANTE F, A. R. Bentivoglio, G. Fabbrini, Fabbrini, G., ABBRUZZESE G, FABBRINI G, Sabetta, A., FABBRINI, Giovanni, Abbruzzese G., Esposito M., A. Guidubaldi, Guidubaldi, A., A. Sabetta, A. Berardelli, Abbruzzese, G., Marinelli, L., MACEROLLO A, G. Defazio, DEFAZIO, Giovanni, SANTORO, LUCIO, Marinelli L., Girlanda P., SANTORO L, D. Liuzzi, Guidubaldi A., LIGUORI R, Defazio G., M. Esposito, Liuzzi D., Bentivoglio, Anna Rita, D. Martino, GUIDUBALDI A, A. Macerollo, ESPOSITO, MARCELLO, L. Marinelli, L. Santoro, Bentivoglio A. R., ESPOSITO, M, R. Liguori, Esposito M, Berardelli, A., MARTINO D, BERARDELLI A, Defazio, G., Sabetta A., Morgante, F., Martino D., LIUZZI D, Bentivoglio, A. R., Martino, D., Macerollo, A., BENTIVOGLIO AR, Liguori, R., Morgante F., P. Girlanda, ABBRUZZESE, GIOVANNI, G. Abbruzzese, MARINELLI L, F. Morgante, Macerollo A., Santoro, L., MARINELLI, LUCIO, BERARDELLI, Alfredo, Berardelli A., DEFAZIO G, Santoro L.   +72 more
core   +1 more source