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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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acute kidney injuryResearch

A multicentre retrospective study investigates the incidence of acute kidney injury in adult patients with hematologic malignancies undergoing vancomycin treatment. The findings contribute to understanding the risks associated with antibiotic therapy in this vulnerable patient population.

acute kidney injury during vancomycin treatment in adult patients with haematologic malignancies a multicentre retrospective study

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Acute Kidney Injury During Vancomycin Treatment in Adult Patients With Haematologic Malignancies: A Multicentre Retrospective Study.”

Gene therapy breakthrough restores heart function in inherited heart disease - reNEW

Gene & Cell Therapy·2 months ago·Read at source →

cholangiocarcinoma hilar cholangiocarcinoma+1 moreResearch

Research from the GLOBAL-BTC registry reveals that chronic liver disease correlates with earlier-stage diagnosis of cholangiocarcinoma and better prognosis. These findings could influence future screening and treatment strategies for patients.

chronic liver disease is associated with earlier stage cholangiocarcinoma diagnosis and improved prognosis findings from the global btc registry

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Chronic liver disease is associated with earlier-stage cholangiocarcinoma diagnosis and improved prognosis: Findings from the GLOBAL-BTC registry.”

colorectal cancerResearch

A recent study reveals a connection between specific bacterial taxa and histological subtypes of colorectal cancer through integrative microbiome-methylome analysis. This research could inform future therapeutic strategies and diagnostics for colorectal cancer.

integrative microbiome methylome analysis links bacterial taxa to colorectal cancer histological subtypes

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Integrative microbiome-methylome analysis links bacterial taxa to colorectal cancer histological subtypes.”

Research

Correction: Caregiver-reported disease burden in Krabbe disease: evaluating outcomes of hematopoietic stem cell transplantation.

PubMed Rare Disease·2 months ago·Read at source →

Research

SLC25A38 gene modification mediated by CRISPR/Cas9 in HEK293T cell line.

PubMed Rare Disease·2 months ago·Read at source →

hearing loss disorderResearch

A study published in PubMed examines the long-term incidence of revision surgery due to electrode migration in cochlear implant patients. The research highlights the effectiveness of a titanium fixation clip applied using a novel reverse application technique.

long term incidence of revision surgery caused by electrode migration in a large cochlear implant cohort using a titanium fixation clip applied by a novel reverse application technique

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Long-term Incidence of Revision Surgery Caused by Electrode Migration in a Large Cochlear Implant Cohort Using a Titanium Fixation Clip Applied by a Novel Reverse Application Technique.”

Research

Recent research highlights the potential of microbial and bioengineered platforms as living drug carriers for precision therapeutic and immunomodulatory delivery. These innovative approaches could redefine treatment strategies for various diseases.

living drug carriers microbial and bioengineered platforms redefining precision therapeutic and immunomodulatory delivery

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Living drug carriers: Microbial and bioengineered platforms redefining precision therapeutic and immunomodulatory delivery.”

Research

A matched-cohort analysis evaluates outcomes of restorative proctectomy and ileal pouch-anal anastomosis across robotic, laparoscopic, and open surgical techniques. The study provides insights into surgical efficacy and patient recovery, contributing to the understanding of surgical options for patients.

outcomes of restorative proctectomy and ileal pouch anal anastomosis a matched cohort analysis of robot assisted laparoscopic and open surgery

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Outcomes of restorative proctectomy and ileal pouch-anal anastomosis: a matched-cohort analysis of robot-assisted, laparoscopic, and open surgery.”

sympathetic ophthalmia proliferative diabetic retinopathy+1 moreResearch

A recent study highlights the diagnostic and therapeutic challenges of sympathetic ophthalmia in patients with proliferative diabetic retinopathy during pregnancy. This research underscores the complexities faced by healthcare providers in managing these conditions simultaneously.

sympathetic ophthalmia complicating proliferative diabetic retinopathy diagnostic and therapeutic challenges during pregnancy

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Sympathetic ophthalmia complicating proliferative diabetic retinopathy: diagnostic and therapeutic challenges during pregnancy.”

systemic lupus erythematosus systemic lupus erythematosus related to C1QA+1 moreResearch

Research highlights that MxA expression in myocarditis associated with systemic lupus erythematosus indicates activation of the type I interferon pathway. This finding could provide insights into the underlying mechanisms of myocarditis in lupus patients.

mxa expression in systemic lupus erythematosus associated myocarditis indicates type i interferon pathway activation

PubMed Rare Disease·2 months ago·Read at source →

Original title: “MxA expression in systemic lupus erythematosus -associated myocarditis indicates type I interferon pathway activation.”

stroke disorderResearch

Recent cohort studies suggest that rare adverse events, such as stroke incidence following COVID-19 vaccination, may be underestimated. This highlights the need for more comprehensive monitoring of vaccine safety in rare disease contexts.

cohort studies may underestimate rare vaccine adverse events evidence from stroke incidence following covid 19 vaccination

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Cohort studies may underestimate rare vaccine adverse events: evidence from stroke incidence following COVID-19 vaccination.”

familial primary hypomagnesemia with hypercalciuria and nephrocalcinosisResearch

A novel variant in the CLDN19 gene has been identified as a cause of familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement. This discovery enhances understanding of the genetic basis of this rare condition.

familial hypomagnesemia with hypercalciuria and nephrocalcinosis fhhnc with ocular involvement due to a novel cldn19 variant

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement due to a novel CLDN19 variant.”

thalassemia beta-thalassemia HBB/LCRBResearch

A decade-long study reveals the genetic epidemiological profile of thalassemia in the childbearing-age population of Huizhou, Guangdong, China. This research provides valuable insights into the prevalence and genetic factors associated with thalassemia in this region.

decade long genetic epidemiological profile of thalassemia in the childbearing age population of huizhou a major hakka center in guangdong china

PubMed Rare Disease·2 months ago·Read at source →

Original title: “A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China.”

ataxia telangiectasia ataxia - telangiectasia variantResearch

A longitudinal study published in PubMed examines neurological disease progression in adults with ataxia telangiectasia. The findings contribute to understanding the disease's impact on adult patients over time.

neurological disease progression in adults with ataxia telangiectasia a longitudinal study

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Neurological disease progression in adults with ataxia telangiectasia: a longitudinal study.”

actinic keratosisResearch

A multicenter real-world study identifies predictors of outcomes and patient satisfaction with tirbanibulin in treating actinic keratosis. The findings may inform treatment strategies and improve patient care in this condition.

predictors of outcomes and satisfaction with tirbanibulin in actinic keratosis a multicenter real world study

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Predictors of outcomes and satisfaction with tirbanibulin in actinic keratosis: a multicenter real-world study.”

hereditary angioedemaResearch

A recent study evaluates deucrictibant as a potential treatment for hereditary angioedema, highlighting its therapeutic promise. The findings contribute to the ongoing research efforts aimed at improving management strategies for this rare condition.

evaluating deucrictibant for the treatment of hereditary angioedema

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Evaluating deucrictibant for the treatment of hereditary angioedema.”

Research

A systematic review evaluates the safety and efficacy of laser and light-based therapies for inflammatory dermatoses, providing insights for cosmetic applications. The findings aim to inform practitioners about potential adverse effects and treatment outcomes.

laser and light based therapies in inflammatory dermatoses a systematic review of safety efficacy and adverse effects to inform cosmetic use

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Laser and Light-Based Therapies in Inflammatory Dermatoses: A Systematic Review of Safety, Efficacy, and Adverse Effects to Inform Cosmetic Use.”

eczematous dermatitis of eyelid atopic eczema+1 moreResearch

A new study explores eczema phenotype clustering in patients with inborn errors of immunity and atopy, aiming to enhance understanding of these conditions. This research could inform future therapeutic strategies and patient management.

eczema phenotype clustering in inborn errors of immunity with atopy toward better understanding

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Eczema phenotype clustering in inborn errors of immunity with atopy: toward better understanding.”

amyotrophic lateral sclerosisResearch

Recent research highlights the role of neuroinflammation in amyotrophic lateral sclerosis (ALS) and emphasizes the potential of precision medicine approaches. This study could pave the way for targeted therapies that address the underlying mechanisms of ALS.

bridging the gap neuroinflammation and the dawn of precision medicine in amyotrophic lateral sclerosis

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Bridging the gap: neuroinflammation and the dawn of precision medicine in amyotrophic lateral sclerosis.”

Previous142 / 482Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A multicentre retrospective study investigates the incidence of acute kidney injury in adult patients with hematologic malignancies undergoing vancomycin treatment. The findings contribute to understanding the risks associated with antibiotic therapy in this vulnerable patient population.

Gene therapy breakthrough restores heart function in inherited heart disease - reNEW

Research from the GLOBAL-BTC registry reveals that chronic liver disease correlates with earlier-stage diagnosis of cholangiocarcinoma and better prognosis. These findings could influence future screening and treatment strategies for patients.

A recent study reveals a connection between specific bacterial taxa and histological subtypes of colorectal cancer through integrative microbiome-methylome analysis. This research could inform future therapeutic strategies and diagnostics for colorectal cancer.

Correction: Caregiver-reported disease burden in Krabbe disease: evaluating outcomes of hematopoietic stem cell transplantation.

SLC25A38 gene modification mediated by CRISPR/Cas9 in HEK293T cell line.

A study published in PubMed examines the long-term incidence of revision surgery due to electrode migration in cochlear implant patients. The research highlights the effectiveness of a titanium fixation clip applied using a novel reverse application technique.

Recent research highlights the potential of microbial and bioengineered platforms as living drug carriers for precision therapeutic and immunomodulatory delivery. These innovative approaches could redefine treatment strategies for various diseases.

A recent study highlights the diagnostic and therapeutic challenges of sympathetic ophthalmia in patients with proliferative diabetic retinopathy during pregnancy. This research underscores the complexities faced by healthcare providers in managing these conditions simultaneously.

Research highlights that MxA expression in myocarditis associated with systemic lupus erythematosus indicates activation of the type I interferon pathway. This finding could provide insights into the underlying mechanisms of myocarditis in lupus patients.

Recent cohort studies suggest that rare adverse events, such as stroke incidence following COVID-19 vaccination, may be underestimated. This highlights the need for more comprehensive monitoring of vaccine safety in rare disease contexts.

A novel variant in the CLDN19 gene has been identified as a cause of familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement. This discovery enhances understanding of the genetic basis of this rare condition.

A decade-long study reveals the genetic epidemiological profile of thalassemia in the childbearing-age population of Huizhou, Guangdong, China. This research provides valuable insights into the prevalence and genetic factors associated with thalassemia in this region.

A longitudinal study published in PubMed examines neurological disease progression in adults with ataxia telangiectasia. The findings contribute to understanding the disease's impact on adult patients over time.

A multicenter real-world study identifies predictors of outcomes and patient satisfaction with tirbanibulin in treating actinic keratosis. The findings may inform treatment strategies and improve patient care in this condition.

A recent study evaluates deucrictibant as a potential treatment for hereditary angioedema, highlighting its therapeutic promise. The findings contribute to the ongoing research efforts aimed at improving management strategies for this rare condition.

A systematic review evaluates the safety and efficacy of laser and light-based therapies for inflammatory dermatoses, providing insights for cosmetic applications. The findings aim to inform practitioners about potential adverse effects and treatment outcomes.

A new study explores eczema phenotype clustering in patients with inborn errors of immunity and atopy, aiming to enhance understanding of these conditions. This research could inform future therapeutic strategies and patient management.

Recent research highlights the role of neuroinflammation in amyotrophic lateral sclerosis (ALS) and emphasizes the potential of precision medicine approaches. This study could pave the way for targeted therapies that address the underlying mechanisms of ALS.

Not rare diseases news,
news about your rare disease.