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

Newsroom9,718 Trends

Daily Briefings

20 earlier

Filter & sort

Source

Sort by

Earlier

20 stories

Research

A narrative review explores the molecular pathways and clinical applications of probiotics in supporting intestinal, neurologic, and cardiovascular health. This research highlights the potential of probiotics as therapeutic agents in these areas.

molecular pathways and clinical applications of probiotics as effective supporters of intestinal neurologic and cardiovascular health a narrative review

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Molecular Pathways and Clinical Applications of Probiotics as Effective Supporters of Intestinal, Neurologic, and Cardiovascular Health: a Narrative Review.”

Research

A clinical analysis of 66 cases with orbital apex syndrome provides insights into the condition's presentation and management. This case series contributes to the understanding of this rare disease, potentially guiding future research and treatment approaches.

clinical analysis of 66 cases with orbital apex syndrome a case series

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Clinical analysis of 66 cases with orbital apex syndrome: a case series.”

Research

A study reports two cases of liver transplantation in children with Type I Abernethy malformation and liver tumors, highlighting different portal vein reconstruction strategies. This research contributes to the understanding of surgical approaches in rare liver conditions.

liver transplantation for type i abernethy malformation with liver tumors in children a report of two cases with contrasting portal vein reconstruction strategies

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Liver transplantation for Type I Abernethy malformation with liver tumors in children: a report of two cases with contrasting portal vein reconstruction strategies.”

Research

A recent study published in PubMed explores the contrasting ancestry patterns in Nanjing people, utilizing Y chromosome and mitochondrial DNA analysis. This research contributes to understanding genetic diversity in southwestern China.

contrasting ancestry patterns inferred from y chromosome and mitochondrial dna in nanjing people from southwestern china

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Contrasting ancestry patterns inferred from Y chromosome and mitochondrial DNA in Nanjing people from southwestern China.”

Research

A narrative review highlights the importance of real-world data and evidence in enhancing the evidence base for precision medicine in the U.S. This approach aims to improve treatment outcomes and patient care in rare diseases.

strengthening the evidence base for precision medicine through the utilization of real world data and real world evidence a narrative review from the u s perspective

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Strengthening the evidence base for precision medicine through the utilization of real-world data and real-world evidence: a narrative review from the U.S. perspective.”

cholesteatoma maxillary sinus cholesteatoma+1 moreResearch

A recent study highlights the diagnostic challenges and surgical management of primary external auditory canal cholesteatoma in young adults. This rare otologic condition requires careful consideration due to its unique presentation and potential complications.

primary external auditory canal cholesteatoma in a young adult diagnostic challenges and surgical management of a rare otologic entity

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Primary external auditory canal cholesteatoma in a young adult: Diagnostic challenges and surgical management of a rare otologic entity.”

Research

New research identifies clinically isolated joint involvement as a distinct entity in Whipple's disease. This finding may enhance understanding and diagnosis of the disease, which is often underrecognized.

clinically isolated joint involvement is a distinct entity in whipple s disease

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Clinically isolated joint involvement is a distinct entity in Whipple's disease.”

lissencephaly spectrum disordersResearch

A recent study published in PubMed examines the long-term neurodevelopmental outcomes and quality of life in patients with lissencephaly related to specific genes including LIS1, PAFAH1B1, DCX, DYNC1H1, TUBA1A, and TUBG1. The findings provide valuable insights into the gene-specific trajectories of these patients.

gene specific long term course neurodevelopmental outcome and quality of life in patients with lis1 pafah1b1 dcx dync1h1 tuba1a and tubg1 related lissencephaly

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly.”

spinal muscular atrophy infantile-onset X-linked spinal muscular atrophyResearch

A recent study published in PubMed analyzes the long-term effects of AAV9-mediated gene replacement therapies for spinal muscular atrophy in mice. This research contributes to understanding the efficacy and safety of gene therapies targeting this rare disease.

long term comparative analysis of aav9 mediated gene replacement therapies for spinal muscular atrophy in mice

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Long-term comparative analysis of AAV9-mediated gene replacement therapies for spinal muscular atrophy in mice.”

prostate cancer prostate cancer, hereditary+1 moreResearch

A new interpretable model using ¹⁸F-PSMA PET/CT-MRI has been developed to enhance decision-making in prostate biopsy procedures. This advancement aims to improve diagnostic accuracy and patient outcomes in prostate cancer management.

interpretable 1 f psma pet ct mri model for optimizing prostate biopsy decisions

PubMed Rare Disease·6 months ago·Read at source →

Original title: “An interpretable (1)⁸F-PSMA PET/CT-MRI model for optimizing prostate biopsy decisions.”

Research

A scoping review highlights the need for improved transition care for young individuals with rare bone and mineral conditions. The findings emphasize the importance of tailored support during the transition from pediatric to adult healthcare services.

transition care for young people with rare bone and mineral conditions a scoping review

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Transition Care for Young People with Rare Bone and Mineral Conditions: A Scoping Review.”

hepatocellular carcinoma pediatric hepatocellular carcinoma+1 moreResearch

A case report highlights a collision tumor of hepatocellular carcinoma and cholangiocarcinoma demonstrating an excellent therapeutic response. This study contributes to the understanding of treatment outcomes for this rare tumor type.

hepatocellular carcinoma cholangiocarcinoma collision tumor with excellent therapeutic response a case report and literature review

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Hepatocellular carcinoma-cholangiocarcinoma collision tumor with excellent therapeutic response: a case report and literature review.”

hypersensitivity pneumonitis hypersensitivity pneumonitis, familial+1 moreResearch

A new study explores cyst-predominant nonfibrotic hypersensitivity pneumonitis, which can mimic Birt-Hogg-Dubé syndrome. This research may enhance diagnostic accuracy for these conditions.

cyst predominant nonfibrotic hypersensitivity pneumonitis mimicking birt hogg dub syndrome

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Cyst-predominant nonfibrotic hypersensitivity pneumonitis mimicking Birt-Hogg-Dubé syndrome.”

arteriovenous malformations of the brainResearch

A systematic review and meta-analysis explores the connection between cerebral arteriovenous malformations and heart diseases in children. This research provides insights that could inform future studies and clinical approaches.

relation between cerebral arteriovenous malformations and heart diseases in the pediatric population a systematic review and meta analysis

PubMed Rare Disease·6 months ago·Read at source →

Original title: “The relation between cerebral arteriovenous malformations and heart diseases in the pediatric population: a systematic review and meta-analysis.”

familial primary hypomagnesemiaResearch

A recent study shows that dapagliflozin effectively corrects hypomagnesemia in kidney transplant patients. This finding could influence treatment protocols for managing magnesium levels post-transplant.

dapagliflozin corrects hypomagnesemia in kidney transplant patients

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Dapagliflozin corrects hypomagnesemia in kidney-transplant patients.”

aplastic anemia idiopathic aplastic anemiaResearch

A new nomogram has been developed and validated for early prognostic prediction in children with aplastic anemia undergoing cyclosporine monotherapy. This tool aims to enhance treatment outcomes by providing timely prognostic insights.

development and validation of a nomogram for early prognostic prediction in childhood aplastic anemia receiving cyclosporine monotherapy

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Development and validation of a nomogram for early prognostic prediction in childhood aplastic anemia receiving cyclosporine monotherapy.”

Research

A qualitative analysis highlights barriers to access for advanced therapy medicinal products (ATMPs) in Europe, emphasizing the need for improved pathways to ensure these therapies reach patients. Stakeholder insights reveal critical gaps in the current system affecting cell therapy distribution.

why promising atmps fail to reach patients a qualitative stakeholder informed analysis of cell therapy access in europe

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Why promising ATMPs fail to reach patients: a qualitative stakeholder-informed analysis of cell therapy access in Europe.”

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

A case-based review highlights the occurrence of diffuse splenic calcifications in patients with systemic lupus erythematosus. This research contributes to the understanding of rare manifestations associated with the disease.

diffuse splenic calcifications in systemic lupus erythematosus a case based review

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Diffuse splenic calcifications in systemic lupus erythematosus: a case-based review.”

Burkitt lymphoma small intestinal Burkitt lymphoma+1 moreResearch

A case report details the successful surgical correction of biatrial cardiac extension of Burkitt lymphoma, highlighting a rare presentation of this aggressive cancer. This case contributes to the understanding of treatment options for patients with unusual manifestations of Burkitt lymphoma.

biatrial cardiac extension of burkitt lymphoma a case report of successful surgical correction

PubMed Rare Disease·6 months ago·Read at source →

Original title: “BiatriaL cardiac extension of Burkitt lymphoma: a case report of successful surgical correction.”

stroke disorderResearch

A retrospective study investigates the impact of deep medullary vein drainage on unfavorable outcomes in stroke patients following endovascular therapy. The findings contribute to understanding the complexities of stroke management and potential complications.

deep medullary vein drainage and unfavorable outcomes in stroke patients after endovascular therapy a retrospective study

PubMed Rare Disease·6 months ago·Read at source →

Original title: “Deep medullary vein drainage and unfavorable outcomes in stroke patients after endovascular therapy: a retrospective study.”

Previous285 / 486Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A narrative review explores the molecular pathways and clinical applications of probiotics in supporting intestinal, neurologic, and cardiovascular health. This research highlights the potential of probiotics as therapeutic agents in these areas.

A clinical analysis of 66 cases with orbital apex syndrome provides insights into the condition's presentation and management. This case series contributes to the understanding of this rare disease, potentially guiding future research and treatment approaches.

A study reports two cases of liver transplantation in children with Type I Abernethy malformation and liver tumors, highlighting different portal vein reconstruction strategies. This research contributes to the understanding of surgical approaches in rare liver conditions.

A recent study published in PubMed explores the contrasting ancestry patterns in Nanjing people, utilizing Y chromosome and mitochondrial DNA analysis. This research contributes to understanding genetic diversity in southwestern China.

A narrative review highlights the importance of real-world data and evidence in enhancing the evidence base for precision medicine in the U.S. This approach aims to improve treatment outcomes and patient care in rare diseases.

A recent study highlights the diagnostic challenges and surgical management of primary external auditory canal cholesteatoma in young adults. This rare otologic condition requires careful consideration due to its unique presentation and potential complications.

New research identifies clinically isolated joint involvement as a distinct entity in Whipple's disease. This finding may enhance understanding and diagnosis of the disease, which is often underrecognized.

A recent study published in PubMed analyzes the long-term effects of AAV9-mediated gene replacement therapies for spinal muscular atrophy in mice. This research contributes to understanding the efficacy and safety of gene therapies targeting this rare disease.

A new interpretable model using ¹⁸F-PSMA PET/CT-MRI has been developed to enhance decision-making in prostate biopsy procedures. This advancement aims to improve diagnostic accuracy and patient outcomes in prostate cancer management.

A scoping review highlights the need for improved transition care for young individuals with rare bone and mineral conditions. The findings emphasize the importance of tailored support during the transition from pediatric to adult healthcare services.

A case report highlights a collision tumor of hepatocellular carcinoma and cholangiocarcinoma demonstrating an excellent therapeutic response. This study contributes to the understanding of treatment outcomes for this rare tumor type.

A new study explores cyst-predominant nonfibrotic hypersensitivity pneumonitis, which can mimic Birt-Hogg-Dubé syndrome. This research may enhance diagnostic accuracy for these conditions.

A systematic review and meta-analysis explores the connection between cerebral arteriovenous malformations and heart diseases in children. This research provides insights that could inform future studies and clinical approaches.

A recent study shows that dapagliflozin effectively corrects hypomagnesemia in kidney transplant patients. This finding could influence treatment protocols for managing magnesium levels post-transplant.

A new nomogram has been developed and validated for early prognostic prediction in children with aplastic anemia undergoing cyclosporine monotherapy. This tool aims to enhance treatment outcomes by providing timely prognostic insights.

A qualitative analysis highlights barriers to access for advanced therapy medicinal products (ATMPs) in Europe, emphasizing the need for improved pathways to ensure these therapies reach patients. Stakeholder insights reveal critical gaps in the current system affecting cell therapy distribution.

A case-based review highlights the occurrence of diffuse splenic calcifications in patients with systemic lupus erythematosus. This research contributes to the understanding of rare manifestations associated with the disease.

A case report details the successful surgical correction of biatrial cardiac extension of Burkitt lymphoma, highlighting a rare presentation of this aggressive cancer. This case contributes to the understanding of treatment options for patients with unusual manifestations of Burkitt lymphoma.

A retrospective study investigates the impact of deep medullary vein drainage on unfavorable outcomes in stroke patients following endovascular therapy. The findings contribute to understanding the complexities of stroke management and potential complications.

Not rare diseases news,
news about your rare disease.