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

Newsroom9,747 Trends

Daily Briefings

20 earlier

Filter & sort

Source

Sort by

Earlier

20 stories

Research

Urine-Derived iPSC Neurospheres Uncover Proteomic Correlates of Clinical Severity in Dravet Syndrome.

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

Research

Q1 earnings take off, Lilly strikes many deals, Regeneron notches historic approval, FDA raises questions

BioSpace·6 months ago·Read at source →

nasopharyngeal carcinomaResearch

A rare case study highlights ovarian metastasis from Epstein-Barr virus-associated undifferentiated nasopharyngeal carcinoma, emphasizing the unusual nature of this occurrence. This discovery contributes to the understanding of metastatic patterns in rare cancers.

ovarian metastasis from ebv associated undifferentiated nasopharyngeal carcinoma an exceptionally rare occurrence

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

Original title: “Ovarian Metastasis from EBV-Associated Undifferentiated Nasopharyngeal Carcinoma: An Exceptionally Rare Occurrence.”

Research

A case report highlights an anthracotic right supraclavicular lymph node that mimicked metastasis in a patient with endometrial carcinosarcoma, as observed through FDG-PET/CT imaging. This finding may influence diagnostic approaches in similar cases.

anthracotic right supraclavicular lymph node mimicking metastasis on fdg pet ct in endometrial carcinosarcoma a case report

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

Original title: “Anthracotic Right Supraclavicular Lymph Node Mimicking Metastasis on FDG-PET/CT in Endometrial Carcinosarcoma: A Case Report.”

breast cancerResearch

A recent case report highlights a rare instance of breast cancer recurrence after 46 years of remission, providing insights into long-term monitoring and treatment implications. This case underscores the need for ongoing vigilance in breast cancer survivors.

breast cancer recurrence after 46 years of remission a case report and clinical implications

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

Original title: “Breast Cancer Recurrence After 46 Years of Remission: A Case Report and Clinical Implications.”

Research

A recent case report details the management of a complex orbital post-transplantation lymphoproliferative disorder, contributing to the understanding of this rare condition. The literature review provides insights into treatment approaches and outcomes.

management of a complex orbital post transplantation lymphoproliferative disorder a case report and literature review

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

Original title: “Management of a Complex Orbital Post-transplantation Lymphoproliferative Disorder: A Case Report and Literature Review.”

Research

A detailed case report reveals new pathological insights into biomarkers for hepatic neuroendocrine tumors, suggesting potential for multimodal therapeutic approaches. This research could enhance understanding and treatment strategies for this rare cancer type.

new pathological insights into biomarkers for multimodal therapeutic approach in hepatic neuroendocrine tumors a detailed case report

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

Original title: “New Pathological Insights into Biomarkers for Multimodal Therapeutic Approach in Hepatic Neuroendocrine Tumors: A Detailed Case Report.”

Research

A new RNA targeting therapy has been developed for a potassium channel linked to severe childhood epilepsy and premature death. This research highlights potential therapeutic avenues for addressing this critical condition.

rna targeting therapy for a prenatally enriched potassium channel associated with severe childhood epilepsy and premature death

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

Original title: “RNA targeting therapy for a prenatally enriched potassium channel associated with severe childhood epilepsy and premature death.”

pulmonary fibrosisResearch

The FIBRONEER-ILD trial evaluates the efficacy and safety of nerandomilast in patients with autoimmune disease-related progressive pulmonary fibrosis. Results indicate potential benefits for this patient population, although further details on outcomes are needed.

efficacy and safety of nerandomilast in patients with autoimmune disease related progressive pulmonary fibrosis in the fibroneer ild trial

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

Original title: “Efficacy and safety of nerandomilast in patients with autoimmune disease-related progressive pulmonary fibrosis in the FIBRONEER-ILD trial.”

amyloidosisResearch

A recent case report highlights acute kidney injury associated with interstitial hemorrhage in patients with renal heavy chain amyloidosis. This study provides valuable insights into the clinicopathologic features of this rare condition.

acute kidney injury with interstitial hemorrhage in renal heavy chain amyloidosis a clinicopathologic case report

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

Original title: “Acute kidney injury with interstitial hemorrhage in renal heavy chain amyloidosis: a clinicopathologic case report.”

Research

A new study explores functional non-coding variations in human genomes using advanced haplotyping and deep learning techniques. This research could enhance understanding of genetic contributions to various diseases.

mapping functional non coding variation in individual human genomes through haplotyping multiomics and deep learning

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

Original title: “Mapping functional non-coding variation in individual human genomes through haplotyping, multiomics, and deep learning.”

myositis disease myositis fibrosa+1 moreResearch

A recent study highlights the complexities of diagnosing and treating calcinosis cutis and delayed-onset myositis in a patient with suspected localized scleroderma. This case underscores the need for careful evaluation in rare disease presentations.

calcinosis cutis and delayed onset myositis in a case of suspected localized scleroderma a diagnostic and therapeutic challenge

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

Original title: “Calcinosis Cutis and Delayed-Onset Myositis in a Case of Suspected Localized Scleroderma: A Diagnostic and Therapeutic Challenge.”

bronchopulmonary dysplasiaResearch

A retrospective cohort study investigates the link between red blood cell transfusions and bronchopulmonary dysplasia in preterm infants. The findings contribute to understanding potential risk factors for this serious condition.

association of red blood cell transfusions with bronchopulmonary dysplasia in preterm infants a retrospective cohort study

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

Original title: “Association of red blood cell transfusions with bronchopulmonary dysplasia in preterm infants: a retrospective cohort study.”

cutaneous tuberculosis primary cutaneous tuberculosisResearch

A recent study highlights chronic perianal ulcerations as a potential manifestation of cutaneous tuberculosis in adults. This finding may prompt further investigation into the dermatological presentations of tuberculosis.

chronic perianal ulcerations over the buttocks in an adult an insidious manifestation of cutaneous tuberculosis

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

Original title: “Chronic perianal ulcerations over the buttocks in an adult: an insidious manifestation of cutaneous tuberculosis.”

deficiency of adenosine deaminase 2Research

A recent study published in PubMed explores multisystem vasculopathy associated with adenosine deaminase 2 deficiency. This research contributes to the understanding of the disease's pathophysiology and potential therapeutic targets.

multisystem vasculopathy in deficiency of adenosine deaminase 2

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

Original title: “Multisystem vasculopathy in deficiency of adenosine deaminase 2.”

Research

Recent research highlights a novel method for prime assembly using linear DNA donors, facilitating large genomic insertions. This breakthrough could enhance gene therapy approaches for various genetic disorders.

prime assembly with linear dna donors enables large genomic insertions

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

Original title: “Prime assembly with linear DNA donors enables large genomic insertions.”

uveitis paraneoplastic uveitis+1 moreResearch

A new study explores the role of anti-vascular endothelial growth factor therapy in treating uveitis, highlighting its potential to address both inflammation and vascular pathology. This research could pave the way for improved therapeutic strategies in managing this condition.

anti vascular endothelial growth factor therapy in uveitis bridging inflammation and vascular pathology

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

Original title: “Anti-vascular endothelial growth factor therapy in uveitis: Bridging inflammation and vascular pathology.”

infective endocarditis Mycoplasma pneumoniae pneumoniaResearch

A case report details infective endocarditis in a child caused by Mycoplasma pneumoniae, highlighting a rare but significant association. This finding may prompt further research into the implications of Mycoplasma infections in pediatric cardiac conditions.

case report of infective endocarditis caused by mycoplasma pneumoniae in a child

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

Original title: “A case report of infective endocarditis caused by Mycoplasma pneumoniae in a child.”

Research

A recent study published in PubMed highlights a case of cystoisospora belli infection in an immunocompetent patient, contributing to the understanding of this rare parasitic disease. This case may provide insights into the clinical presentation and management of cystoisospora belli infections.

cystoisospora belli infection in an immunocompetent patient

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

Original title: “Cystoisospora belli infection in an immunocompetent patient.”

necrobiosis lipoidicaResearch

A nonrandomized clinical trial investigates a deuterated pentoxifylline analog for treating necrobiosis lipoidica. The study contributes to understanding potential therapeutic options for this rare skin condition.

deuterated pentoxifylline analog in the treatment of necrobiosis lipoidica a nonrandomized clinical trial

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

Original title: “Deuterated Pentoxifylline Analog in the Treatment of Necrobiosis Lipoidica: A Nonrandomized Clinical Trial.”

Previous336 / 488Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

Urine-Derived iPSC Neurospheres Uncover Proteomic Correlates of Clinical Severity in Dravet Syndrome.

Q1 earnings take off, Lilly strikes many deals, Regeneron notches historic approval, FDA raises questions

A rare case study highlights ovarian metastasis from Epstein-Barr virus-associated undifferentiated nasopharyngeal carcinoma, emphasizing the unusual nature of this occurrence. This discovery contributes to the understanding of metastatic patterns in rare cancers.

A case report highlights an anthracotic right supraclavicular lymph node that mimicked metastasis in a patient with endometrial carcinosarcoma, as observed through FDG-PET/CT imaging. This finding may influence diagnostic approaches in similar cases.

A recent case report highlights a rare instance of breast cancer recurrence after 46 years of remission, providing insights into long-term monitoring and treatment implications. This case underscores the need for ongoing vigilance in breast cancer survivors.

A recent case report details the management of a complex orbital post-transplantation lymphoproliferative disorder, contributing to the understanding of this rare condition. The literature review provides insights into treatment approaches and outcomes.

A detailed case report reveals new pathological insights into biomarkers for hepatic neuroendocrine tumors, suggesting potential for multimodal therapeutic approaches. This research could enhance understanding and treatment strategies for this rare cancer type.

A new RNA targeting therapy has been developed for a potassium channel linked to severe childhood epilepsy and premature death. This research highlights potential therapeutic avenues for addressing this critical condition.

The FIBRONEER-ILD trial evaluates the efficacy and safety of nerandomilast in patients with autoimmune disease-related progressive pulmonary fibrosis. Results indicate potential benefits for this patient population, although further details on outcomes are needed.

A recent case report highlights acute kidney injury associated with interstitial hemorrhage in patients with renal heavy chain amyloidosis. This study provides valuable insights into the clinicopathologic features of this rare condition.

A new study explores functional non-coding variations in human genomes using advanced haplotyping and deep learning techniques. This research could enhance understanding of genetic contributions to various diseases.

A recent study highlights the complexities of diagnosing and treating calcinosis cutis and delayed-onset myositis in a patient with suspected localized scleroderma. This case underscores the need for careful evaluation in rare disease presentations.

A retrospective cohort study investigates the link between red blood cell transfusions and bronchopulmonary dysplasia in preterm infants. The findings contribute to understanding potential risk factors for this serious condition.

A recent study highlights chronic perianal ulcerations as a potential manifestation of cutaneous tuberculosis in adults. This finding may prompt further investigation into the dermatological presentations of tuberculosis.

A recent study published in PubMed explores multisystem vasculopathy associated with adenosine deaminase 2 deficiency. This research contributes to the understanding of the disease's pathophysiology and potential therapeutic targets.

Recent research highlights a novel method for prime assembly using linear DNA donors, facilitating large genomic insertions. This breakthrough could enhance gene therapy approaches for various genetic disorders.

A new study explores the role of anti-vascular endothelial growth factor therapy in treating uveitis, highlighting its potential to address both inflammation and vascular pathology. This research could pave the way for improved therapeutic strategies in managing this condition.

A case report details infective endocarditis in a child caused by Mycoplasma pneumoniae, highlighting a rare but significant association. This finding may prompt further research into the implications of Mycoplasma infections in pediatric cardiac conditions.

A recent study published in PubMed highlights a case of cystoisospora belli infection in an immunocompetent patient, contributing to the understanding of this rare parasitic disease. This case may provide insights into the clinical presentation and management of cystoisospora belli infections.

A nonrandomized clinical trial investigates a deuterated pentoxifylline analog for treating necrobiosis lipoidica. The study contributes to understanding potential therapeutic options for this rare skin condition.

Not rare diseases news,
news about your rare disease.