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

Newsroom9,770 Trends

Daily Briefings

20 earlier

Filter & sort

Source

Sort by

Earlier

20 stories

breast cancerResearch

A recent study explores the resistance mechanisms of trastuzumab deruxtecan in HER2-amplified versus HER2-low breast cancer. Understanding these differences could inform treatment strategies and improve patient outcomes.

different diseases different escapes trastuzumab deruxtecan resistance in her2 amplified versus her2 low breast cancer

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Different Diseases, Different Escapes: Trastuzumab Deruxtecan Resistance in HER2-Amplified versus HER2-Low Breast Cancer.”

multisystem inflammatory syndrome in children and adults COVID-19–associated multisystem inflammatory syndrome in childrenResearch

A case study highlights endomyocardial calcification associated with pulmonary and systemic hypertension in a neonate diagnosed with multisystem inflammatory syndrome of newborn (MIS-N). This research contributes to understanding the cardiovascular implications of MIS-N in infants.

endomyocardial calcification with pulmonary and systemic hypertension in a term neonate with multisystem inflammatory syndrome of newborn mis n

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Endomyocardial calcification with pulmonary and systemic hypertension in a term neonate with multisystem inflammatory syndrome of newborn (MIS-N).”

Research

A study published in PubMed explores the gut microbiome diversity and functional profiles of Culicoides in Sanya, Ruili, and Linyi, China. This research may provide insights into the ecological roles of these insects and their potential impact on disease transmission.

gut microbiome diversity and functional profiles of culicoides across sanya ruili and linyi china

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Gut microbiome diversity and functional profiles of Culicoides across Sanya, Ruili, and Linyi, China.”

glycogen storage disease II glycogen storage disease III+1 moreResearch

A retrospective study investigates the correlation between biochemical and imaging markers and hepatic adenoma in patients with glycogen storage disease. This research provides insights that could enhance diagnostic approaches for this rare condition.

correlation of biochemical and imaging markers with hepatic adenoma in patients with glycogen storage disease a retrospective single center study

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Correlation of biochemical and imaging markers with hepatic adenoma in patients with glycogen storage disease: a retrospective single-center study.”

Research

Recent research highlights the association between TNF inhibitor therapy and overlapping autoimmunity and demyelination syndromes. This study provides insights into potential adverse effects that may impact treatment decisions for patients receiving TNF inhibitors.

overlapping autoimmunity and demyelination syndromes associated with tnf inhibitor therapy

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Overlapping autoimmunity and demyelination syndromes associated with TNF inhibitor therapy.”

cervical intraepithelial neoplasia cervical intraepithelial neoplasia grade 2/3+1 moreResearch

A rare case report highlights the association of HPV-16 with hematocervix and hematometra, leading to cervical intraepithelial neoplasia (CIN). This study contributes to the understanding of HPV's role in rare gynecological conditions.

hematocervix and hematometra a rare case report of hpv 16 induced cervical intraepithelial neoplasia cin

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Hematocervix and Hematometra: A Rare Case Report of HPV-16 Induced Cervical Intraepithelial Neoplasia (CIN).”

Research

A case report details an ectopic maxillary ACTH-secreting adenoma leading to Nelson's syndrome. This study contributes to the understanding of rare endocrine disorders and their complications.

ectopic maxillary acth secreting adenoma complicated by nelson s syndrome a case report

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Ectopic maxillary ACTH-secreting adenoma complicated by Nelson's syndrome: a case report.”

melanomaResearch

A new study investigates the potential of cfDNA fragmentomics as a biomarker for melanoma in real-world patients. This research could enhance early detection and monitoring strategies for melanoma.

exploring global cfdna fragmentomics as a biomarker in real world melanoma patients

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Exploring global cfDNA fragmentomics as a biomarker in real-world melanoma patients.”

Research

A recent study discusses the challenges of ovarian stimulation and oocyte cryopreservation in a patient with Hirata syndrome, highlighting the complexities in assisted reproduction for this rare condition. The findings may inform future clinical practices in fertility preservation.

ovarian stimulation toward oocyte cryopreservation for fertility preservation in a patient with hirata syndrome a clinical challenge in assisted reproduction

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Ovarian stimulation toward oocyte cryopreservation for fertility preservation in a patient with Hirata syndrome: a clinical challenge in assisted reproduction.”

cholesteatoma maxillary sinus cholesteatoma+1 moreResearch

A recent case study highlights the occurrence of external auditory canal cholesteatoma in a teenager, shedding light on this rare condition. The findings emphasize the need for awareness and early diagnosis to prevent complications.

hidden peril in the ear a case of external auditory canal cholesteatoma in a teenager

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Hidden Peril in the Ear: A Case of External Auditory Canal Cholesteatoma in a Teenager.”

Epstein-Barr virus infection congenital Epstein-Barr virus infectionResearch

A case study highlights the presence of phagocytic mesothelial cells in pericardial effusion after allogeneic peripheral blood stem cell transplantation for chronic active Epstein-Barr virus infection. This research provides new insights into the cytomorphological and immunocytochemical characteristics associated with this rare condition.

phagocytic mesothelial cells in pericardial effusion following allogeneic peripheral blood stem cell transplantation for chronic active epstein barr virus infection a distinctive cytomorphological and immunocytochemical case study

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Phagocytic Mesothelial Cells in Pericardial Effusion Following Allogeneic Peripheral Blood Stem Cell Transplantation for Chronic Active Epstein-Barr Virus Infection: A Distinctive Cytomorphological and Immunocytochemical Case Study.”

idiopathic acute eosinophilic pneumoniaResearch

A new study published in PubMed explores the natural history of patients with histologically proven acute eosinophilic myocarditis. This research provides insights into the disease's progression and patient outcomes, contributing to the understanding of this rare condition.

natural history of patients with histologically proven acute eosinophilic myocarditis

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Natural History of Patients With Histologically Proven Acute Eosinophilic Myocarditis.”

peripheral neuropathy peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome+1 moreResearch

A systematic review and meta-analysis reveals the global prevalence of peripheral neuropathy in cancer patients post-chemotherapy. This study highlights the significant impact of chemotherapy on nerve health, emphasizing the need for better management strategies.

global prevalence of peripheral neuropathy following chemotherapy in cancer patients a systematic review and meta analysis

PubMed Rare Disease·9 months ago·Read at source →

Original title: “The global prevalence of peripheral neuropathy following chemotherapy in cancer patients: a systematic review and meta-analysis.”

Research

A five-case series highlights venous adventitial cystic disease of the lower extremities, which can mimic deep vein thrombosis. This research contributes to the understanding of this rare condition and its clinical implications.

venous adventitial cystic disease of the lower extremities mimicking deep vein thrombosis a five case series

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Venous Adventitial Cystic Disease of the Lower Extremities Mimicking Deep Vein Thrombosis: A Five-Case Series.”

pyoderma gangrenosum pyoderma gangrenosum-acne-suppurative hidradenitis syndromeResearch

A rare case report details fasciitis-like primary breast pyoderma gangrenosum, contributing to the understanding of this uncommon condition. This study may provide insights for clinicians dealing with similar rare dermatological cases.

fasciitis like primary breast pyoderma gangrenosum a rare case report

PubMed Rare Disease·9 months ago·Read at source →

Original title: “[Fasciitis-like primary breast pyoderma gangrenosum: A rare case report].”

Research

A new study presents a method for the single-round evolution of RNA aptamers using GRAPE-LM, potentially enhancing the development of targeted therapies. This research could lead to advancements in precision medicine for various conditions.

single round evolution of rna aptamers with grape lm

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Single-round evolution of RNA aptamers with GRAPE-LM.”

Research

A new study presents a weakly supervised transformer model designed for diagnosing rare diseases and subphenotyping using electronic health records (EHRs). The research focuses on pulmonary case studies, potentially enhancing diagnostic accuracy in rare disease identification.

weakly supervised transformer for rare disease diagnosis and subphenotyping from ehrs with pulmonary case studies

PubMed Rare Disease·9 months ago·Read at source →

Original title: “A weakly supervised transformer for rare disease diagnosis and subphenotyping from EHRs with pulmonary case studies.”

Fabry diseaseResearch

A recent study highlights the significant cardiovascular morbidity and mortality associated with Fabry disease. This research underscores the need for increased awareness and targeted interventions for patients suffering from this rare condition.

cardiovascular morbidity and mortality in fabry disease

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Cardiovascular Morbidity and Mortality in Fabry Disease.”

primary pulmonary diffuse large B-cell lymphoma MALT lymphomaResearch

A recent study highlights primary pulmonary MALT lymphoma as a rare condition often misdiagnosed due to its pneumonic presentation. This research underscores the need for increased awareness and accurate diagnosis of this rare lymphoma subtype.

silent imposter in pneumonic attire primary pulmonary malt lymphoma

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Silent imposter in pneumonic attire: primary pulmonary MALT lymphoma.”

Research

A study analyzing stillbirths at a Shanghai maternity center from 2014 to 2024 reveals trends in sex distribution and gestational age-specific risks. The findings contribute to understanding factors influencing stillbirth rates.

stillbirths in a large shanghai maternity centre 2014 2024 trends sex distribution and gestational age specific risk

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Stillbirths in a large Shanghai maternity centre (2014-2024): trends, sex distribution, and gestational age-specific risk.”

Previous473 / 489Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A recent study explores the resistance mechanisms of trastuzumab deruxtecan in HER2-amplified versus HER2-low breast cancer. Understanding these differences could inform treatment strategies and improve patient outcomes.

A case study highlights endomyocardial calcification associated with pulmonary and systemic hypertension in a neonate diagnosed with multisystem inflammatory syndrome of newborn (MIS-N). This research contributes to understanding the cardiovascular implications of MIS-N in infants.

A study published in PubMed explores the gut microbiome diversity and functional profiles of Culicoides in Sanya, Ruili, and Linyi, China. This research may provide insights into the ecological roles of these insects and their potential impact on disease transmission.

A retrospective study investigates the correlation between biochemical and imaging markers and hepatic adenoma in patients with glycogen storage disease. This research provides insights that could enhance diagnostic approaches for this rare condition.

Recent research highlights the association between TNF inhibitor therapy and overlapping autoimmunity and demyelination syndromes. This study provides insights into potential adverse effects that may impact treatment decisions for patients receiving TNF inhibitors.

A rare case report highlights the association of HPV-16 with hematocervix and hematometra, leading to cervical intraepithelial neoplasia (CIN). This study contributes to the understanding of HPV's role in rare gynecological conditions.

A case report details an ectopic maxillary ACTH-secreting adenoma leading to Nelson's syndrome. This study contributes to the understanding of rare endocrine disorders and their complications.

A new study investigates the potential of cfDNA fragmentomics as a biomarker for melanoma in real-world patients. This research could enhance early detection and monitoring strategies for melanoma.

A recent study discusses the challenges of ovarian stimulation and oocyte cryopreservation in a patient with Hirata syndrome, highlighting the complexities in assisted reproduction for this rare condition. The findings may inform future clinical practices in fertility preservation.

A recent case study highlights the occurrence of external auditory canal cholesteatoma in a teenager, shedding light on this rare condition. The findings emphasize the need for awareness and early diagnosis to prevent complications.

A new study published in PubMed explores the natural history of patients with histologically proven acute eosinophilic myocarditis. This research provides insights into the disease's progression and patient outcomes, contributing to the understanding of this rare condition.

A systematic review and meta-analysis reveals the global prevalence of peripheral neuropathy in cancer patients post-chemotherapy. This study highlights the significant impact of chemotherapy on nerve health, emphasizing the need for better management strategies.

A five-case series highlights venous adventitial cystic disease of the lower extremities, which can mimic deep vein thrombosis. This research contributes to the understanding of this rare condition and its clinical implications.

A rare case report details fasciitis-like primary breast pyoderma gangrenosum, contributing to the understanding of this uncommon condition. This study may provide insights for clinicians dealing with similar rare dermatological cases.

A new study presents a method for the single-round evolution of RNA aptamers using GRAPE-LM, potentially enhancing the development of targeted therapies. This research could lead to advancements in precision medicine for various conditions.

A new study presents a weakly supervised transformer model designed for diagnosing rare diseases and subphenotyping using electronic health records (EHRs). The research focuses on pulmonary case studies, potentially enhancing diagnostic accuracy in rare disease identification.

A recent study highlights the significant cardiovascular morbidity and mortality associated with Fabry disease. This research underscores the need for increased awareness and targeted interventions for patients suffering from this rare condition.

A recent study highlights primary pulmonary MALT lymphoma as a rare condition often misdiagnosed due to its pneumonic presentation. This research underscores the need for increased awareness and accurate diagnosis of this rare lymphoma subtype.

A study analyzing stillbirths at a Shanghai maternity center from 2014 to 2024 reveals trends in sex distribution and gestational age-specific risks. The findings contribute to understanding factors influencing stillbirth rates.

Not rare diseases news,
news about your rare disease.