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What's new in your rare disease | Kisho

Not rare diseases news,
news about your rare disease.

Every story we pull is tagged to the disease it’s about — so you can filter to your condition and read only what matters.

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eosinophilic granulomatosis with polyangiitisResearch

Recent research highlights the role of eosinophils in the pathobiology of eosinophilic granulomatosis with polyangiitis, suggesting potential therapeutic strategies. This study provides insights into the immunologic mechanisms underlying the disease and future treatment avenues.

eosinophils in the immunologic spectrum of eosinophilic granulomatosis with polyangiitis from fundamental pathobiology to emerging therapeutic strategies and future perspectives

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Eosinophils in the immunologic spectrum of Eosinophilic Granulomatosis with Polyangiitis: From Fundamental Pathobiology to Emerging Therapeutic Strategies and Future Perspectives.”

mast cell activation syndrome idiopathic mast cell activation syndrome+1 moreResearch

New insights into mast cell activation syndrome (MCAS) have emerged with the six-year update on the global consensus-2 diagnostic criteria. This progress aims to enhance diagnostic accuracy and patient management for those affected by this rare condition.

progress in mast cell activation syndrome the global consensus 2 diagnostic criteria at six years

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Progress in mast cell activation syndrome: the global consensus-2 diagnostic criteria at six years.”

Research

A recent case report details Mounier Kuhn Syndrome, contributing to the understanding of this rare condition. The findings may aid in diagnosis and management strategies for affected patients.

mounier kuhn syndrome a case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Mounier Kuhn Syndrome - A Case Report.”

toxic epidermal necrolysisResearch

A new cohort study investigates the prevalence and risk factors associated with epidermal necrolysis sequelae. This research contributes to understanding the long-term impacts of this severe skin condition.

epidermal necrolysis sequelae a cohort study on prevalence and risk factors

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Epidermal necrolysis sequelae: A cohort study on prevalence and risk factors.”

tetralogy of fallot tetralogy of fallot and glaucomaResearch

A case report details the successful intracardiac repair of unrepaired tetralogy of Fallot in a 51-year-old woman. This highlights potential surgical options for adult patients with this congenital heart defect.

successful intracardiac repair of unrepaired tetralogy of fallot in a 51 year old woman a case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Successful intracardiac repair of unrepaired tetralogy of fallot in a 51-year-old woman: a case report.”

Research

A study explores the use of transcranial direct current stimulation (tDCS) as a treatment for drug-resistant hallucinations in adolescents. This research could pave the way for new therapeutic approaches in managing severe psychiatric symptoms.

transcranial direct current stimulation to treat drug resistant hallucinations in adolescents

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Transcranial direct current stimulation to treat drug-resistant hallucinations in adolescents.”

Research

A case report details a young adult with primary splenic angiosarcoma presenting with unexplained anemia. This study contributes to the understanding of this rare cancer's clinical presentation.

primary splenic angiosarcoma presenting with unexplained anemia in a young adult a case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Primary splenic angiosarcoma presenting with unexplained anemia in a young adult: a case report.”

Research

A case report details triple-vessel coronary involvement and a giant aneurysm in a 6-year-old boy with Kawasaki disease. This study highlights the severe cardiovascular complications that can arise from Kawasaki disease, emphasizing the need for early detection and management.

triple vessel coronary involvement and giant aneurysm in a 6 year old boy with kawasaki disease a case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Triple-vessel coronary involvement and giant aneurysm in a 6-year-old boy with kawasaki disease: a case report.”

steroid inherited metabolic disorderResearch

A recent study focuses on optimizing formulations of Levocarnitine for pediatric patients with inherited metabolic disorders. This research highlights the importance of tailored treatments to improve therapeutic outcomes in this vulnerable population.

optimising formulations for paediatric patients with inherited metabolic disorders the case study of levocarnitine

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Optimising Formulations for Paediatric Patients with Inherited Metabolic Disorders: The Case Study of Levocarnitine.”

melanoma erythema nodosum+1 moreResearch

A recent study highlights the occurrence of erythema nodosum-like panniculitis in patients undergoing BRAF inhibitor therapy for melanoma, emphasizing the need to consider latent tuberculosis infection in these cases. This research adds to the understanding of skin reactions associated with targeted cancer therapies.

erythema nodosum like panniculitis during braf inhibitor therapy for melanoma never forget latent tuberculosis infection

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Erythema nodosum-like panniculitis during BRAF inhibitor therapy for melanoma: never forget latent tuberculosis infection.”

rheumatic disease of mitral valve rheumatic pulmonary valve diseaseResearch

A recent study highlights the risks associated with glucocorticoid therapy in patients with rheumatic diseases undergoing surgery. The findings emphasize the need for careful management to mitigate potential complications during surgical procedures.

risks and management of glucocorticoid therapy for patients with rheumatic disease having surgery

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Risks and Management of Glucocorticoid Therapy for Patients with Rheumatic Disease Having Surgery.”

Research

A new study explores methods for analyzing paired case-control data to compare predictive values, potentially enhancing the understanding of rare diseases. This research could inform future studies and improve predictive modeling in clinical settings.

analyze paired case control data prospectively in comparing two predictive values

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Analyze paired case-control data prospectively in comparing two predictive values.”

Research

A pictorial review highlights interlobular septal thickening, providing insights into its radiological features. This review may aid in the diagnosis and understanding of related pulmonary conditions.

interlobular septal thickening a pictorial review

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Interlobular Septal Thickening: A Pictorial Review.”

Research

A study identifies the CHMP2B p.Ala30Ser variant as a potential modifier in early-onset Alzheimer's disease, suggesting its role in endolysosomal dysfunction. This discovery could inform future research on therapeutic targets for Alzheimer's.

chmp2b p ala30ser variant in biomarker confirmed early onset alzheimer disease a potential endolysosomal disease modifier

PubMed Rare Disease·5 months ago·Read at source →

Original title: “CHMP2B p.Ala30Ser Variant in Biomarker-Confirmed Early-Onset Alzheimer Disease: A Potential Endolysosomal Disease Modifier.”

schwannoma schwannomatosisResearch

A case report highlights multiple cervical vagus nerve schwannomas that were misidentified as abnormal lymph nodes during sonography. This finding underscores the need for careful imaging interpretation in rare nerve tumors.

multiple cervical vagus nerve schwannomas masquerading as abnormal lymph nodes in sonography a case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Multiple Cervical Vagus Nerve Schwannomas Masquerading as Abnormal Lymph Nodes in Sonography: A Case Report.”

intravenous leiomyomatosisResearch

A recent publication reports two cases of uterine leiomyomas with intravenous leiomyomatosis, contributing to the understanding of this rare condition. The findings may inform future research and clinical approaches to managing similar cases.

uterine leiomyomas with intravenous leiomyomatosis a report of two cases

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Uterine Leiomyomas with Intravenous Leiomyomatosis: A Report of Two Cases.”

thrombotic microangiopathyResearch

A new case series published on renal-limited thrombotic microangiopathy in infants provides insights into this rare condition. The findings may enhance understanding and management of the disease in pediatric populations.

renal limited thrombotic microangiopathy in infants a case series

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Renal-Limited Thrombotic Microangiopathy in Infants: A Case Series.”

Research

A recent study compares gemcitabine-based chemotherapy to fluoropyrimidine-based chemotherapy for first-line palliative treatment in advanced ampullary adenocarcinoma. The research highlights the potential role of platinum combinations in improving treatment outcomes.

gemcitabine based versus fluoropyrimidine based chemotherapy and role of platinum combination for first line palliative systemic treatment in advanced ampullary adenocarcinoma

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Gemcitabine-Based versus Fluoropyrimidine-Based Chemotherapy and Role of Platinum Combination for First-Line Palliative Systemic Treatment in Advanced Ampullary Adenocarcinoma.”

omphalocele, autosomal omphalocele+1 moreResearch

A case report highlights an unusual omphalocele associated with Cantrell syndrome, contributing to the understanding of this rare condition. This report may provide insights for clinicians dealing with similar cases.

unusual omphalocele a case report of cantrell syndrome

PubMed Rare Disease·5 months ago·Read at source →

Original title: “An unusual omphalocele: a case report of Cantrell syndrome.”

Turner syndrome Wilson-Turner syndromeResearch

A rare case report details the co-occurrence of moyamoya syndrome and Turner syndrome in a 4-year-old girl from Sudan. This case highlights the complexities of diagnosing and managing multiple rare conditions simultaneously.

co occurrence of moyamoya syndrome and turner syndrome in a 4 year old sudanese girl a rare case report

PubMed Rare Disease·5 months ago·Read at source →

Original title: “Co-occurrence of moyamoya syndrome and Turner syndrome in a 4-year-old Sudanese girl: a rare case report.”

Previous263 / 486Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

Recent research highlights the role of eosinophils in the pathobiology of eosinophilic granulomatosis with polyangiitis, suggesting potential therapeutic strategies. This study provides insights into the immunologic mechanisms underlying the disease and future treatment avenues.

New insights into mast cell activation syndrome (MCAS) have emerged with the six-year update on the global consensus-2 diagnostic criteria. This progress aims to enhance diagnostic accuracy and patient management for those affected by this rare condition.

A recent case report details Mounier Kuhn Syndrome, contributing to the understanding of this rare condition. The findings may aid in diagnosis and management strategies for affected patients.

A new cohort study investigates the prevalence and risk factors associated with epidermal necrolysis sequelae. This research contributes to understanding the long-term impacts of this severe skin condition.

A case report details the successful intracardiac repair of unrepaired tetralogy of Fallot in a 51-year-old woman. This highlights potential surgical options for adult patients with this congenital heart defect.

A study explores the use of transcranial direct current stimulation (tDCS) as a treatment for drug-resistant hallucinations in adolescents. This research could pave the way for new therapeutic approaches in managing severe psychiatric symptoms.

A case report details a young adult with primary splenic angiosarcoma presenting with unexplained anemia. This study contributes to the understanding of this rare cancer's clinical presentation.

A case report details triple-vessel coronary involvement and a giant aneurysm in a 6-year-old boy with Kawasaki disease. This study highlights the severe cardiovascular complications that can arise from Kawasaki disease, emphasizing the need for early detection and management.

A recent study focuses on optimizing formulations of Levocarnitine for pediatric patients with inherited metabolic disorders. This research highlights the importance of tailored treatments to improve therapeutic outcomes in this vulnerable population.

A recent study highlights the risks associated with glucocorticoid therapy in patients with rheumatic diseases undergoing surgery. The findings emphasize the need for careful management to mitigate potential complications during surgical procedures.

A new study explores methods for analyzing paired case-control data to compare predictive values, potentially enhancing the understanding of rare diseases. This research could inform future studies and improve predictive modeling in clinical settings.

A pictorial review highlights interlobular septal thickening, providing insights into its radiological features. This review may aid in the diagnosis and understanding of related pulmonary conditions.

A study identifies the CHMP2B p.Ala30Ser variant as a potential modifier in early-onset Alzheimer's disease, suggesting its role in endolysosomal dysfunction. This discovery could inform future research on therapeutic targets for Alzheimer's.

A case report highlights multiple cervical vagus nerve schwannomas that were misidentified as abnormal lymph nodes during sonography. This finding underscores the need for careful imaging interpretation in rare nerve tumors.

A recent publication reports two cases of uterine leiomyomas with intravenous leiomyomatosis, contributing to the understanding of this rare condition. The findings may inform future research and clinical approaches to managing similar cases.

A new case series published on renal-limited thrombotic microangiopathy in infants provides insights into this rare condition. The findings may enhance understanding and management of the disease in pediatric populations.

A recent study compares gemcitabine-based chemotherapy to fluoropyrimidine-based chemotherapy for first-line palliative treatment in advanced ampullary adenocarcinoma. The research highlights the potential role of platinum combinations in improving treatment outcomes.

A case report highlights an unusual omphalocele associated with Cantrell syndrome, contributing to the understanding of this rare condition. This report may provide insights for clinicians dealing with similar cases.

A rare case report details the co-occurrence of moyamoya syndrome and Turner syndrome in a 4-year-old girl from Sudan. This case highlights the complexities of diagnosing and managing multiple rare conditions simultaneously.

Not rare diseases news,
news about your rare disease.