Explore Diseases Find Orgs Patient Assistance News Insights About

Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

Open rare disease resources — free, sourced, never gated.

Resources

Rare Disease Directory
Patient Organization Directory
Patient Assistance Programs
Rare Disease News
Clinical Trials
Research Publications

Legal

Privacy Policy
Terms of Service
Accessibility
About & Methodology
Contact

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.

News sourcesFDA·NIH·CDC·EMA·PubMed·Federal Register·NORD·EURORDIS·Global Genes·The Mighty·BioPharma Dive·BioSpace

Newsroom9,628 Trends

Daily Briefings

20 earlier

Filter & sort

Source

Sort by

Earlier

20 stories

Research

A recent publication discusses the role of artificial intelligence in diagnosing and managing rare diseases in Latin America. It highlights both the opportunities and challenges faced in implementing AI technologies in this context.

artificial intelligence in the diagnosis treatment and management of rare diseases opportunities and challenges from a latin american perspective

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Artificial Intelligence in the Diagnosis, Treatment, and Management of Rare Diseases: Opportunities and Challenges from a Latin American Perspective.”

congenital primary aphakiaResearch

A new study explores corneal morphometrics in congenital primary aphakia using multimodal imaging techniques. This research could enhance understanding of the disease and inform future therapeutic strategies.

corneal morphometrics in congenital primary aphakia a multimodal imaging perspective

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Corneal Morphometrics in Congenital Primary Aphakia: A Multimodal Imaging Perspective.”

Research

A recent study compares retifanlimab and avelumab for treating metastatic Merkel cell carcinoma using a matching-adjusted indirect comparison analysis. This research contributes to understanding treatment options for this aggressive skin cancer.

retifanlimab versus avelumab for the treatment of metastatic merkel cell carcinoma a matching adjusted indirect comparison analysis

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Retifanlimab Versus Avelumab for the Treatment of Metastatic Merkel Cell Carcinoma: A Matching-Adjusted Indirect Comparison Analysis.”

Research

Recent research highlights next-generation immune cell engagers designed for B cell depletion in autoimmune diseases. These advancements could lead to more effective treatments for conditions characterized by B cell dysregulation.

next generation immune cell engagers for b cell depletion in autoimmune diseases

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Next-generation immune cell engagers for B cell depletion in autoimmune diseases.”

postpartum psychosis alcoholic psychosis+1 moreResearch

A recent study highlights altered pain processing and neural circuitry disruptions in adolescents with early-onset psychosis. This research could inform future therapeutic strategies for managing pain in this population.

altered pain processing and associated neural circuitry disruptions in adolescents with early onset psychosis

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Altered pain processing and associated neural circuitry disruptions in adolescents with early-onset psychosis.”

Research

A new publication outlines a comprehensive set of value assessment criteria aimed at guiding funders in drug repurposing initiatives. This framework is designed to enhance decision-making processes in the context of rare diseases.

defining a comprehensive set of value assessment criteria for funders of drug repurposing initiatives

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Defining a comprehensive set of value assessment criteria for funders of drug repurposing initiatives.”

Research

A systematic review highlights the clinical features of cough syncope, providing insights into its diagnosis and management. This research may aid clinicians in recognizing and treating this rare condition more effectively.

clinical features of cough syncope a systematic review

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Clinical features of cough syncope: a systematic review.”

Research

A 16-week real-world study evaluates the efficacy and safety of delgocitinib for adults with moderate-to-severe chronic hand eczema. The findings highlight the drug's impact on patient perspectives, providing valuable insights into treatment outcomes.

efficacy and safety of delgocitinib and its impact on patient s perspective for moderate to severe chronic hand eczema in adults a 16 week real world prospective multicentre study

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Efficacy and Safety of Delgocitinib and Its Impact on Patient's Perspective for Moderate-to-severe Chronic Hand Eczema in Adults: A 16-week Real-world Prospective Multicentre Study.”

Research

Recent research identifies two truncating variants in the MITF gene that broaden the phenotypic spectrum of COMMAD syndrome. This discovery enhances understanding of the genetic underpinnings of the condition.

two truncating mitf variants expand the phenotypic spectrum of commad syndrome

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.”

Burkitt lymphoma small intestinal Burkitt lymphoma+1 moreResearch

A case study highlights scleral perforation in a young adult diagnosed with Burkitt lymphoma, contributing to the understanding of ocular complications associated with this aggressive cancer. This research adds to the body of knowledge regarding rare disease manifestations.

scleral perforation in a young adult with burkitt lymphoma

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Scleral perforation in a young adult with Burkitt lymphoma.”

Research

A new podcast discusses the advancements and perspectives on immune checkpoint inhibitors in treating Merkel cell carcinoma over the past decade. This highlights ongoing research and developments in therapeutic strategies for this rare skin cancer.

perspectives on 10 years of immune checkpoint inhibitors in merkel cell carcinoma a podcast

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Perspectives on 10 years of Immune Checkpoint Inhibitors in Merkel Cell Carcinoma: A Podcast.”

Research

A new study explores the spectral characteristics and parameters of pulse oximetry waveforms, providing insights into their potential for assessing resuscitation status. This research could enhance monitoring techniques in critical care settings.

spectral characteristics and parameters of pulse oximetry waveforms for assessing resuscitation status

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Spectral Characteristics and Parameters of Pulse Oximetry Waveforms for Assessing Resuscitation Status.”

Moyamoya disease moyamoya disease 7+1 moreResearch

A case study highlights the occurrence of Fregoli syndrome in an adolescent diagnosed with Moyamoya disease. This research adds to the understanding of the neurological implications associated with Moyamoya disease.

fregoli syndrome in an adolescent with moyamoya disease

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Fregoli syndrome in an adolescent with Moyamoya disease.”

aortic valve stenosis subvalvular aortic stenosis+1 moreResearch

Recent research highlights the link between sudden cardiac death and aortic stenosis, emphasizing the need for increased awareness and early intervention. This study provides valuable insights into the mechanisms underlying this serious condition.

sudden cardiac death due to aortic stenosis

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Sudden cardiac death due to aortic stenosis.”

psoriatic arthritisResearch

The 5-year results from the Phase 3 SELECT-PsA 1 study demonstrate the long-term safety and efficacy of Upadacitinib in patients with psoriatic arthritis. This data provides valuable insights into the sustained benefits of this treatment over an extended period.

long term safety and efficacy of upadacitinib in patients with psoriatic arthritis 5 year results from the phase 3 select psa 1 study

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Long-Term Safety and Efficacy of Upadacitinib in Patients with Psoriatic Arthritis: 5-Year Results from the Phase 3 SELECT-PsA 1 Study.”

hypophosphatasia infantile hypophosphatasia+1 moreResearch

A systematic review highlights the prevalence of hypophosphatasia across general and specific patient populations. This research provides valuable insights into the disease's occurrence, which may inform future studies and treatment approaches.

prevalence of hypophosphatasia in general and selected patient populations a systematic review

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Prevalence of hypophosphatasia in general and selected patient populations: a systematic review.”

Alexander disease Alexander disease type I+1 moreResearch

A recent case report details the diagnosis of Alexander disease in an obstetrics patient, contributing to the understanding of this rare condition. The report includes a review of existing literature, highlighting the complexities of diagnosing Alexander disease in atypical presentations.

alexander disease diagnosed in an obstetrics patient a case report and review of the literature

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Alexander Disease Diagnosed in an Obstetrics Patient: A Case Report and Review of the Literature.”

long COVID-19Research

A cross-sectional study from the SOMA.COV research highlights the prevalence and factors associated with somatic symptom disorder in patients suffering from post COVID-19 condition. This research provides insights into the psychological impacts of long COVID, which may inform future treatment approaches.

frequency and correlates of somatic symptom disorder in patients with post covid 19 condition cross sectional results from the soma cov study

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Frequency and correlates of somatic symptom disorder in patients with post COVID-19 condition: Cross-sectional results from the SOMA.COV study.”

classic Kaposi sarcoma colon Kaposi sarcomaResearch

A case study highlights the rare occurrence of ileal Kaposi sarcoma in a transplant recipient alongside Crohn's disease, presenting with subocclusive symptoms. This finding underscores the complexity of managing concomitant rare diseases in patients.

beyond crohn s disease ileal kaposi sarcoma in a transplant recipient presenting with subocclusive symptoms a concomitant diagnosis of crohn s disease and ileal kaposi sarcoma

PubMed Rare Disease·29 days ago·Read at source →

Original title: “Beyond Crohn's disease: ileal Kaposi sarcoma in a transplant recipient presenting with subocclusive symptoms. A concomitant diagnosis of Crohn's disease and ileal Kaposi sarcoma.”

congenitalResearch

A recent study highlights the significant burden of congenital erythropoietic porphyria, an ultra-rare inherited skin disorder. The findings underscore the need for increased awareness and research into this condition.

burden of an ultra rare inherited skin disorder congenital erythropoietic porphyria

PubMed Rare Disease·29 days ago·Read at source →

Original title: “The burden of an ultra-rare inherited skin disorder: Congenital erythropoietic porphyria.”

Previous50 / 482Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A recent publication discusses the role of artificial intelligence in diagnosing and managing rare diseases in Latin America. It highlights both the opportunities and challenges faced in implementing AI technologies in this context.

A new study explores corneal morphometrics in congenital primary aphakia using multimodal imaging techniques. This research could enhance understanding of the disease and inform future therapeutic strategies.

A recent study compares retifanlimab and avelumab for treating metastatic Merkel cell carcinoma using a matching-adjusted indirect comparison analysis. This research contributes to understanding treatment options for this aggressive skin cancer.

Recent research highlights next-generation immune cell engagers designed for B cell depletion in autoimmune diseases. These advancements could lead to more effective treatments for conditions characterized by B cell dysregulation.

A recent study highlights altered pain processing and neural circuitry disruptions in adolescents with early-onset psychosis. This research could inform future therapeutic strategies for managing pain in this population.

A new publication outlines a comprehensive set of value assessment criteria aimed at guiding funders in drug repurposing initiatives. This framework is designed to enhance decision-making processes in the context of rare diseases.

A systematic review highlights the clinical features of cough syncope, providing insights into its diagnosis and management. This research may aid clinicians in recognizing and treating this rare condition more effectively.

A 16-week real-world study evaluates the efficacy and safety of delgocitinib for adults with moderate-to-severe chronic hand eczema. The findings highlight the drug's impact on patient perspectives, providing valuable insights into treatment outcomes.

Recent research identifies two truncating variants in the MITF gene that broaden the phenotypic spectrum of COMMAD syndrome. This discovery enhances understanding of the genetic underpinnings of the condition.

A case study highlights scleral perforation in a young adult diagnosed with Burkitt lymphoma, contributing to the understanding of ocular complications associated with this aggressive cancer. This research adds to the body of knowledge regarding rare disease manifestations.

A new podcast discusses the advancements and perspectives on immune checkpoint inhibitors in treating Merkel cell carcinoma over the past decade. This highlights ongoing research and developments in therapeutic strategies for this rare skin cancer.

A new study explores the spectral characteristics and parameters of pulse oximetry waveforms, providing insights into their potential for assessing resuscitation status. This research could enhance monitoring techniques in critical care settings.

A case study highlights the occurrence of Fregoli syndrome in an adolescent diagnosed with Moyamoya disease. This research adds to the understanding of the neurological implications associated with Moyamoya disease.

Recent research highlights the link between sudden cardiac death and aortic stenosis, emphasizing the need for increased awareness and early intervention. This study provides valuable insights into the mechanisms underlying this serious condition.

The 5-year results from the Phase 3 SELECT-PsA 1 study demonstrate the long-term safety and efficacy of Upadacitinib in patients with psoriatic arthritis. This data provides valuable insights into the sustained benefits of this treatment over an extended period.

A systematic review highlights the prevalence of hypophosphatasia across general and specific patient populations. This research provides valuable insights into the disease's occurrence, which may inform future studies and treatment approaches.

A recent case report details the diagnosis of Alexander disease in an obstetrics patient, contributing to the understanding of this rare condition. The report includes a review of existing literature, highlighting the complexities of diagnosing Alexander disease in atypical presentations.

A case study highlights the rare occurrence of ileal Kaposi sarcoma in a transplant recipient alongside Crohn's disease, presenting with subocclusive symptoms. This finding underscores the complexity of managing concomitant rare diseases in patients.

A recent study highlights the significant burden of congenital erythropoietic porphyria, an ultra-rare inherited skin disorder. The findings underscore the need for increased awareness and research into this condition.

Not rare diseases news,
news about your rare disease.