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What's new in your rare disease | Kisho

Not rare diseases news,
news about your rare disease.

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periprosthetic joint infectionResearch

A case report highlights a periprosthetic joint infection caused by Salmonella species occurring two years post unicompartmental knee arthroplasty. The infection was managed with debridement, antibiotics, and implant retention, contributing to the understanding of rare infection management in orthopedic procedures.

periprosthetic joint infection with salmonella species 2 years after unicompartmental knee arthroplasty treated with debridement antibiotics and implant retention dair a case report and review of the literature

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Periprosthetic Joint Infection With Salmonella Species 2 Years After Unicompartmental Knee Arthroplasty Treated With Debridement, Antibiotics, and Implant Retention (DAIR): A Case Report and Review of the Literature.”

Research

A recent study published in PubMed explores the association between transferrin levels and clinical outcomes in patients with ANCA-associated vasculitis. This research may provide insights into potential biomarkers for disease management.

association of transferrin levels with clinical outcomes in anca associated vasculitis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Association of transferrin levels with clinical outcomes in ANCA-associated vasculitis.”

osteonecrosis of the jaw rheumatoid arthritis+1 moreResearch

A recent clinical analysis highlights the risk factors for osteonecrosis of the jaw in patients with rheumatoid arthritis, emphasizing the need for improved oral health management in this population. The findings could inform future research and clinical practices.

clinical analysis of osteonecrosis of the jaw in patients with rheumatoid arthritis risk factors and oral health implications

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Clinical analysis of osteonecrosis of the jaw in patients with rheumatoid arthritis: risk factors and oral health implications.”

inborn error of immunity inborn errors of metabolismResearch

A recent bibliometric analysis highlights emerging trends and research hotspots in inborn errors of immunity. This study provides insights into the evolving landscape of research in this rare disease area.

emerging trends and research hot spots in inborn error of immunity a bibliometric perspective

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Emerging trends and research hot spots in inborn error of immunity: A bibliometric perspective.”

Research

A recent case report details the diagnosis of amoebic peritonitis in a patient suffering from acute intestinal obstruction. This study highlights the importance of recognizing amoebic infections in clinical settings.

diagnosis of amoebic peritonitis in peritoneal fluid in a patient with acute intestinal obstruction a case report

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Diagnosis of Amoebic Peritonitis in Peritoneal Fluid in a Patient With Acute Intestinal Obstruction: A Case Report.”

Research

A study published on PubMed examines 21 cases of osseous hydatidosis, highlighting its clinicopathological and radiological features. This research underscores the diagnostic challenges and therapeutic complexities associated with this rare condition.

osseous hydatidosis a diagnostic mimic and a therapeutic challenge clinicopathological and radiological features of 21 cases from india

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Osseous hydatidosis - A diagnostic mimic and a therapeutic challenge: Clinicopathological and radiological features of 21 cases from India.”

amyotrophic lateral sclerosisResearch

A new study investigates the genetic epidemiology of C9orf72 repeat expansion linked to amyotrophic lateral sclerosis (ALS) in Hungary. This research contributes to understanding the prevalence and genetic factors associated with ALS in this region.

genetic epidemiology of c9orf72 repeat expansion associated amyotrophic lateral sclerosis in hungary

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Genetic epidemiology of C9orf72 repeat expansion associated amyotrophic lateral sclerosis in Hungary.”

Cogan syndromeResearch

A recent publication highlights an unexpected death in a young child with Cogan syndrome, raising concerns about the disease's severity and management. This case underscores the need for further research into Cogan syndrome and its implications for affected individuals.

unexpected death in a young child with cogan syndrome

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Unexpected Death in a Young Child With Cogan Syndrome.”

Research

Recent genomic analysis of Megalocytivirus genomes highlights significant recombination events, which could impact understanding of viral evolution and disease mechanisms. This research contributes to the broader knowledge of viral genetics.

genomic analysis of megalocytivirus genomes reveals widespread recombination

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Genomic analysis of Megalocytivirus genomes reveals widespread recombination.”

methotrexate-associated lymphoproliferative disordersResearch

A new study explores the pathobiology and diagnostic challenges of lymphoproliferative disorders following CAR T cell therapy. The research provides mechanistic insights that could inform future therapeutic strategies.

spectrum pathobiology mechanistic insights and diagnostic challenges of post car t cell therapy lymphoproliferative disorders

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Spectrum, pathobiology, mechanistic insights and diagnostic challenges of post-CAR T cell therapy lymphoproliferative disorders.”

Research

A meta-summary of case reports highlights the occurrence of Twiddler syndrome and Reel syndrome in patients with subcutaneous implantable cardioverter-defibrillators (S-ICD). This research provides insights into the complications associated with S-ICD devices.

twiddler syndrome and reel syndrome in patients with subcutaneous implantable cardioverter defibrillator s icd a meta summary of case reports

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Twiddler syndrome and Reel syndrome in patients with subcutaneous implantable cardioverter-defibrillator (S-ICD): a meta-summary of case reports.”

scrub typhus hydrops fetalis+1 moreResearch

A recent study highlights congenital scrub typhus as a cause of non-immune hydrops fetalis, expanding the understanding of this rare condition. This discovery may influence future diagnostic and treatment approaches for affected pregnancies.

congenital scrub typhus presenting as non immune hydrops fetalis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Congenital scrub typhus presenting as non-immune hydrops fetalis.”

acromegalyResearch

A recent study published in PubMed highlights the disease-related burden and treatment experiences of patients with acromegaly, emphasizing gender differences. The findings provide valuable insights for tailoring treatment approaches to improve patient outcomes.

disease related burden and treatment experience in patients with acromegaly a gender perspective

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Disease-related burden and treatment experience in patients with acromegaly: a gender perspective.”

schizophrenia schizophrenia 15Research

A recent study highlights the growing concern among individuals with schizophrenia regarding the risk of developing Alzheimer's disease. This finding underscores the need for further research into the intersection of these two conditions.

even schizophrenics fear alzheimer s disease

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Even schizophrenics fear Alzheimer's disease.”

Research

A case study highlights successful ECMO-assisted management of Landouzy sepsis in a young adult with multiorgan failure, utilizing an individualized antituberculous regimen. This research contributes to understanding treatment approaches for complex rare diseases.

landouzy sepsis in a young adult with multiorgan failure successful ecmo assisted management using an individualized antituberculous regimen

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Landouzy sepsis in a young adult with multiorgan failure: successful ECMO-assisted management using an individualized antituberculous regimen.”

Research

A case study highlights a metastatic rosette-forming glioneuronal tumor presenting as isolated primary amenorrhea. This research contributes to the understanding of rare tumors and their atypical presentations.

metastatic rosette forming glioneuronal tumour presenting as isolated primary amenorrhoea

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Metastatic rosette-forming glioneuronal tumour presenting as isolated primary amenorrhoea.”

Research

A case report details a rare instance of primary splenic angiosarcoma in a young patient, highlighting the challenges associated with diagnosing and treating this uncommon disease. This report contributes to the limited literature on angiosarcoma, emphasizing the need for increased awareness and research.

case report of primary splenic angiosarcoma in a young patient a very rare and challenging disease

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Case Report of Primary Splenic Angiosarcoma in a Young Patient: A Very Rare and Challenging Disease.”

Research

Recent research identifies new genotype-phenotype correlations for individuals with RERE variants, providing updated management recommendations. These findings enhance understanding of the clinical implications of RERE mutations.

new genotype phenotype correlations and management recommendations for individuals with rere variants

PubMed Rare Disease·7 months ago·Read at source →

Original title: “New genotype-phenotype correlations and management recommendations for individuals with RERE variants.”

Research

50 employees impacted as Astellas closes Universal Cells' Seattle office

BioSpace·7 months ago·Read at source →

Research

FDA Issues Draft Guidance on Genome Editing Safety Standards to Advance Gene Therapy Development

FDA Press Releases·7 months ago·Read at source →

Previous366 / 488Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A recent study published in PubMed explores the association between transferrin levels and clinical outcomes in patients with ANCA-associated vasculitis. This research may provide insights into potential biomarkers for disease management.

A recent clinical analysis highlights the risk factors for osteonecrosis of the jaw in patients with rheumatoid arthritis, emphasizing the need for improved oral health management in this population. The findings could inform future research and clinical practices.

A recent bibliometric analysis highlights emerging trends and research hotspots in inborn errors of immunity. This study provides insights into the evolving landscape of research in this rare disease area.

A recent case report details the diagnosis of amoebic peritonitis in a patient suffering from acute intestinal obstruction. This study highlights the importance of recognizing amoebic infections in clinical settings.

A study published on PubMed examines 21 cases of osseous hydatidosis, highlighting its clinicopathological and radiological features. This research underscores the diagnostic challenges and therapeutic complexities associated with this rare condition.

A new study investigates the genetic epidemiology of C9orf72 repeat expansion linked to amyotrophic lateral sclerosis (ALS) in Hungary. This research contributes to understanding the prevalence and genetic factors associated with ALS in this region.

A recent publication highlights an unexpected death in a young child with Cogan syndrome, raising concerns about the disease's severity and management. This case underscores the need for further research into Cogan syndrome and its implications for affected individuals.

Recent genomic analysis of Megalocytivirus genomes highlights significant recombination events, which could impact understanding of viral evolution and disease mechanisms. This research contributes to the broader knowledge of viral genetics.

A new study explores the pathobiology and diagnostic challenges of lymphoproliferative disorders following CAR T cell therapy. The research provides mechanistic insights that could inform future therapeutic strategies.

A meta-summary of case reports highlights the occurrence of Twiddler syndrome and Reel syndrome in patients with subcutaneous implantable cardioverter-defibrillators (S-ICD). This research provides insights into the complications associated with S-ICD devices.

A recent study highlights congenital scrub typhus as a cause of non-immune hydrops fetalis, expanding the understanding of this rare condition. This discovery may influence future diagnostic and treatment approaches for affected pregnancies.

A recent study published in PubMed highlights the disease-related burden and treatment experiences of patients with acromegaly, emphasizing gender differences. The findings provide valuable insights for tailoring treatment approaches to improve patient outcomes.

A recent study highlights the growing concern among individuals with schizophrenia regarding the risk of developing Alzheimer's disease. This finding underscores the need for further research into the intersection of these two conditions.

A case study highlights successful ECMO-assisted management of Landouzy sepsis in a young adult with multiorgan failure, utilizing an individualized antituberculous regimen. This research contributes to understanding treatment approaches for complex rare diseases.

A case study highlights a metastatic rosette-forming glioneuronal tumor presenting as isolated primary amenorrhea. This research contributes to the understanding of rare tumors and their atypical presentations.

Recent research identifies new genotype-phenotype correlations for individuals with RERE variants, providing updated management recommendations. These findings enhance understanding of the clinical implications of RERE mutations.

50 employees impacted as Astellas closes Universal Cells' Seattle office

FDA Issues Draft Guidance on Genome Editing Safety Standards to Advance Gene Therapy Development

Not rare diseases news,
news about your rare disease.