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

A recent study compares AI diagnostic generators with expert opinions in challenging neurologic diagnoses, highlighting the potential of AI in clinical settings. The findings suggest that AI can enhance diagnostic accuracy, although expert input remains crucial.

comparison of ai diagnostic generator and expert opinion in difficult neurologic diagnosis real world case study

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Comparison of AI, diagnostic generator, and expert opinion in difficult neurologic diagnosis: real-world case study.”

chronic kidney disease polycystic kidney disease 5Research

A rare case study highlights a bloodstream infection caused by Comamonas testosteroni in a patient with stage 5 chronic kidney disease undergoing maintenance hemodialysis. This case underscores the potential for unusual infections in immunocompromised patients.

beyond bioremediation a rare case of comamonas testosteroni bloodstream infection in a patient with stage 5 chronic kidney disease on maintenance hemodialysis

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Beyond Bioremediation: A Rare Case of Comamonas testosteroni Bloodstream Infection in a Patient With Stage 5 Chronic Kidney Disease on Maintenance Hemodialysis.”

Research

A recent study indicates that patients with T-cell/histiocyte-rich large B-cell lymphoma have a low risk of central nervous system relapse, even when presenting with high-risk disease characteristics. This finding could influence treatment strategies and monitoring protocols for this patient population.

low risk of central nervous system relapse among patients with t cell histiocyte rich large b cell lymphoma despite high risk disease presentation

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Low Risk of Central Nervous System Relapse Among Patients With T-Cell/Histiocyte-Rich Large B-Cell Lymphoma Despite High-Risk Disease Presentation.”

atypical teratoid rhabdoid tumor rhabdoid tumor predisposition syndrome 2+1 moreResearch

A case study highlights the use of hemispherotomy in treating drug-resistant epilepsy associated with atypical teratoid rhabdoid tumors. This surgical approach may offer new insights into managing complex cases of epilepsy linked to rare tumors.

hemispherotomy for atypical teratoid rhabdoid tumor associated drug resistant epilepsy illustrative case

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Hemispherotomy for atypical teratoid rhabdoid tumor-associated drug-resistant epilepsy: illustrative case.”

POEMS syndromeResearch

A multicenter study investigates the morphological characteristics of renal lesions in TAFRO syndrome and POEMS syndrome. This research enhances understanding of these rare diseases and may inform future diagnostic and treatment strategies.

morphological characteristics of the renal lesion in tafro syndrome and poems syndrome a retrospective and multicenter study

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Morphological characteristics of the renal lesion in TAFRO syndrome and POEMS syndrome: a retrospective and multicenter study.”

virus-associated trichodysplasia spinulosaResearch

Recent updates on trichodysplasia spinulosa disease provide new insights into its pathogenesis and potential therapeutic approaches. This rare disease, characterized by hair follicle abnormalities, continues to be a focus of ongoing research.

updates on trichodysplasia spinulosa disease

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Updates on Trichodysplasia Spinulosa Disease.”

Research

A recent study highlights the importance of fractionated urine glycosaminoglycans in diagnosing mucopolysaccharidosis type II, based on evaluations from four unrelated families. This research could enhance diagnostic accuracy for this rare condition.

critical role of fractionated urine glycosaminoglycans in the evaluation of mucopolysaccharidosis type ii in four unrelated families

PubMed Rare Disease·7 months ago·Read at source →

Original title: “The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families.”

Research

A recent study expands the clinical and genetic spectrum of fumarase deficiency, highlighting diagnostic challenges in both pediatric and adult patients. This research provides valuable insights that could enhance understanding and management of the disease.

diagnostic conundrum in fumarase deficiency expanding the clinical and genetic spectrum in a cohort of pediatric and adult patients

PubMed Rare Disease·7 months ago·Read at source →

Original title: “A Diagnostic Conundrum in Fumarase Deficiency: Expanding the Clinical and Genetic Spectrum in a Cohort of Pediatric and Adult Patients.”

Research

A new study provides high-resolution genomic characterization of WAGR spectrum disorder, enhancing understanding through a novel cohort and literature synthesis. The research also validates patient-reported data, contributing valuable insights into this rare condition.

high resolution genomic characterization of wagr spectrum disorder insights from a novel cohort and literature synthesis and validation of patient reported data

PubMed Rare Disease·7 months ago·Read at source →

Original title: “High-Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient-Reported Data.”

rheumatoid arthritis polyarticular juvenile rheumatoid arthritisResearch

A real-world observational study in Italy shows that upadacitinib effectively achieves and maintains remission in patients with moderate-to-severe rheumatoid arthritis over one year. This data supports the drug's role in long-term management of the disease.

achievement and maintenance of remission with upadacitinib in patients with moderate to severe rheumatoid arthritis in italy 1 year data from uphold a prospective real world observational study

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Achievement and Maintenance of Remission with Upadacitinib in Patients with Moderate-to-Severe Rheumatoid Arthritis in Italy: 1-Year Data from UPHOLD, a Prospective Real-World Observational Study.”

von Willebrand disease (hereditary or acquired)von Willebrand disease 2+1 moreResearch

A recent study published in PubMed highlights a rare case of mucosal bleeding in a newborn, revealing an unusual combination of Type 2A and Type 2N von Willebrand Disease. This research contributes to the understanding of bleeding disorders in neonates.

mucosal bleeding in a newborn with low factor viii activity an unusual combination of type 2a and type 2n von willebrand disease

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Mucosal Bleeding in a Newborn With Low Factor VIII Activity: An Unusual Combination of Type 2A and Type 2N von Willebrand Disease.”

Fabry diseaseResearch

Researchers in China developed and validated a self-management efficacy questionnaire specifically for patients with Fabry disease. This tool aims to enhance patient engagement and management of their condition.

development and validation of a self management efficacy questionnaire for patients with fabry disease in china

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Development and validation of a self-management efficacy questionnaire for patients with Fabry disease in China.”

heart failure congestive heart failure+1 moreResearch

A recent study highlights the role of oral microbiome dysbiosis in connecting emotional disorders with systemic inflammation in heart failure patients. This research could pave the way for new therapeutic strategies targeting the microbiome in heart failure management.

oral microbiome dysbiosis mediates the link between emotional disorders and systemic inflammation in heart failure

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Oral microbiome dysbiosis mediates the link between emotional disorders and systemic inflammation in heart failure.”

breast cancerResearch

A case report details spontaneous auto-amputation of the breast in a patient with advanced malignant fungating wounds and distant metastases to the lungs and left upper extremity. This unique presentation highlights the severe complications associated with advanced malignancies.

spontaneous auto amputation of the breast in a patient with advanced malignant fungating wound and distant metastases involving the lungs and left upper extremity a case report

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Spontaneous Auto-Amputation of the Breast in a Patient With Advanced Malignant Fungating Wound and Distant Metastases Involving the Lungs and Left Upper Extremity: A Case Report.”

frontal sinus neoplasmResearch

A study published in PubMed discusses a case of frontal mucocele leading to a fronto-mucocutaneous fistula following traditional cautery. This highlights potential complications in sinus surgeries and the need for careful postoperative monitoring.

persistent forehead sinus after traditional cautery frontal mucocele complicated by a fronto mucocutaneous fistula

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Persistent Forehead Sinus After Traditional Cautery: Frontal Mucocele Complicated by a Fronto-Mucocutaneous Fistula.”

COVID-19Research

A recent study published in PubMed explores age-dependent variations in circulating T follicular helper (Tfh) and T follicular regulatory (Tfr) cells following SARS-CoV-2 infection. The findings may provide insights into immune responses across different age groups.

age dependent variations in circulating tfh and tfr cells following sars cov 2 infection

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Age-dependent variations in circulating Tfh and Tfr cells following SARS-CoV-2 infection.”

Research

A recent study highlights the effectiveness of instrumental assessments in tracking movement improvements in patients with Parkinson's disease. This research could enhance monitoring and treatment strategies for this condition.

instrumental assessment of movement series reflects scored improvement of patients with parkinson s disease

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Instrumental assessment of movement series reflects scored improvement of patients with Parkinson's disease.”

pustular psoriasis generalized pustular psoriasisResearch

A recent case series published in PubMed highlights management strategies for juvenile generalized pustular psoriasis in children. The findings contribute to the understanding of treatment approaches for this rare skin condition.

juvenile generalized pustular psoriasis management in children a case series

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Juvenile Generalized Pustular Psoriasis: Management in Children-A Case Series.”

dystrophic pulmonary ossification COVID-19Research

A rare case study highlights the rapid progression and subsequent improvement of pulmonary ossification during COVID-19 pneumonia. This finding contributes to the understanding of pulmonary complications associated with COVID-19.

rare case of pulmonary ossification findings that rapidly progressed and improved during the course of covid 19 pneumonia

PubMed Rare Disease·7 months ago·Read at source →

Original title: “A Rare Case of Pulmonary Ossification Findings That Rapidly Progressed and Improved During the Course of COVID-19 Pneumonia.”

Research

A recent analysis highlights trends in the disease burden of malignant neoplasms of bone and articular cartilage in China from 1990 to 2023. This study, based on the Global Burden of Disease data, provides insights into the evolving landscape of these cancers.

trends and future of the disease burden of malignant neoplasms of bone and articular cartilage in china from 1990 to 2023 an analysis based on the global burden of disease 2023

PubMed Rare Disease·7 months ago·Read at source →

Original title: “Trends and future of the disease burden of malignant neoplasms of bone and articular cartilage in China from 1990 to 2023: An analysis based on the Global Burden of Disease 2023.”

Previous371 / 488Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A recent study compares AI diagnostic generators with expert opinions in challenging neurologic diagnoses, highlighting the potential of AI in clinical settings. The findings suggest that AI can enhance diagnostic accuracy, although expert input remains crucial.

A rare case study highlights a bloodstream infection caused by Comamonas testosteroni in a patient with stage 5 chronic kidney disease undergoing maintenance hemodialysis. This case underscores the potential for unusual infections in immunocompromised patients.

A case study highlights the use of hemispherotomy in treating drug-resistant epilepsy associated with atypical teratoid rhabdoid tumors. This surgical approach may offer new insights into managing complex cases of epilepsy linked to rare tumors.

A multicenter study investigates the morphological characteristics of renal lesions in TAFRO syndrome and POEMS syndrome. This research enhances understanding of these rare diseases and may inform future diagnostic and treatment strategies.

Recent updates on trichodysplasia spinulosa disease provide new insights into its pathogenesis and potential therapeutic approaches. This rare disease, characterized by hair follicle abnormalities, continues to be a focus of ongoing research.

A recent study highlights the importance of fractionated urine glycosaminoglycans in diagnosing mucopolysaccharidosis type II, based on evaluations from four unrelated families. This research could enhance diagnostic accuracy for this rare condition.

A recent study expands the clinical and genetic spectrum of fumarase deficiency, highlighting diagnostic challenges in both pediatric and adult patients. This research provides valuable insights that could enhance understanding and management of the disease.

A new study provides high-resolution genomic characterization of WAGR spectrum disorder, enhancing understanding through a novel cohort and literature synthesis. The research also validates patient-reported data, contributing valuable insights into this rare condition.

A real-world observational study in Italy shows that upadacitinib effectively achieves and maintains remission in patients with moderate-to-severe rheumatoid arthritis over one year. This data supports the drug's role in long-term management of the disease.

A recent study published in PubMed highlights a rare case of mucosal bleeding in a newborn, revealing an unusual combination of Type 2A and Type 2N von Willebrand Disease. This research contributes to the understanding of bleeding disorders in neonates.

Researchers in China developed and validated a self-management efficacy questionnaire specifically for patients with Fabry disease. This tool aims to enhance patient engagement and management of their condition.

A recent study highlights the role of oral microbiome dysbiosis in connecting emotional disorders with systemic inflammation in heart failure patients. This research could pave the way for new therapeutic strategies targeting the microbiome in heart failure management.

A case report details spontaneous auto-amputation of the breast in a patient with advanced malignant fungating wounds and distant metastases to the lungs and left upper extremity. This unique presentation highlights the severe complications associated with advanced malignancies.

A study published in PubMed discusses a case of frontal mucocele leading to a fronto-mucocutaneous fistula following traditional cautery. This highlights potential complications in sinus surgeries and the need for careful postoperative monitoring.

A recent study published in PubMed explores age-dependent variations in circulating T follicular helper (Tfh) and T follicular regulatory (Tfr) cells following SARS-CoV-2 infection. The findings may provide insights into immune responses across different age groups.

A recent study highlights the effectiveness of instrumental assessments in tracking movement improvements in patients with Parkinson's disease. This research could enhance monitoring and treatment strategies for this condition.

A recent case series published in PubMed highlights management strategies for juvenile generalized pustular psoriasis in children. The findings contribute to the understanding of treatment approaches for this rare skin condition.

A rare case study highlights the rapid progression and subsequent improvement of pulmonary ossification during COVID-19 pneumonia. This finding contributes to the understanding of pulmonary complications associated with COVID-19.

A recent analysis highlights trends in the disease burden of malignant neoplasms of bone and articular cartilage in China from 1990 to 2023. This study, based on the Global Burden of Disease data, provides insights into the evolving landscape of these cancers.

Not rare diseases news,
news about your rare disease.