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

hypophosphatemiaResearch

A case report highlights the delayed diagnosis of tumor-induced osteomalacia due to overlooked hypophosphatemia linked to excess fibroblast growth factor 23. This underscores the need for increased awareness and diagnostic vigilance in similar cases.

tumor induced osteomalacia caused by fibroblast growth factor 23 excess delayed diagnosis resulting from overlooked hypophosphatemia a case report

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Tumor-induced osteomalacia caused by fibroblast growth factor 23 excess : Delayed diagnosis resulting from overlooked hypophosphatemia-A case report.”

lymphoma orbit lymphomaResearch

A recent case series published in PubMed highlights instances of spontaneous regression in vitreoretinal lymphoma lesions, contributing to the understanding of this rare condition. The findings may influence future research and treatment approaches for lymphoma.

spontaneous regression of vitreoretinal lymphoma lesions case series and literature review

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Spontaneous Regression of Vitreoretinal Lymphoma Lesions: Case Series and Literature Review.”

chronic kidney disease polycystic kidney disease 5Research

Recent research identifies FAN1 mutations as a contributing factor to karyomegalic nephropathy in chronic kidney disease. This discovery may open new avenues for understanding the genetic basis of kidney disorders.

fan1 mutation and karyomegalic nephropathy in chronic kidney disease

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “FAN1 mutation and karyomegalic nephropathy in chronic kidney disease.”

interstitial lung disease interstitial lung disease 2Research

A recent study highlights pulmonary AL amyloidosis as a significant cause of interstitial lung disease, diagnosed through transbronchial lung biopsy. This discovery may enhance diagnostic accuracy and treatment approaches for affected patients.

pulmonary al amyloidosis as a cause of interstitial lung disease diagnosed with transbronchial lung biopsy

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Pulmonary AL Amyloidosis as a Cause of Interstitial Lung Disease Diagnosed With Transbronchial Lung Biopsy.”

mucosal melanoma head and neck cancerResearch

A new study identifies immunohistochemical predictors for head and neck mucosal melanoma, potentially aiding in diagnosis and treatment strategies. This research contributes to the understanding of biomarkers in this rare cancer type.

immunohistochemical predictors in head and neck mucosal melanoma

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Immunohistochemical Predictors in Head and Neck Mucosal Melanoma.”

Research

A new German S3-level guideline has been published for the diagnosis and management of rare dental disorders. This guideline aims to standardize care and improve outcomes for patients with these conditions.

german s3 level guideline for the diagnosis and management of rare dental disorders

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “The German S3-level guideline for the diagnosis and management of rare dental disorders.”

adrenocortical carcinoma, hereditary pheochromocytoma+1 moreResearch

A recent study highlights the diagnostic challenges of PTHrP-mediated hypercalcemia in metastatic adrenocortical carcinoma, which can mimic pheochromocytoma. This research underscores the need for careful differentiation in clinical settings.

pthrp mediated hypercalcemia in metastatic adrenocortical carcinoma mimicking pheochromocytoma a diagnostic challenge

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “PTHrP-mediated hypercalcemia in metastatic adrenocortical carcinoma mimicking pheochromocytoma: a diagnostic challenge.”

histoplasmosis histoplasmosis retinitis+1 moreResearch

A case study highlights gastric involvement in disseminated histoplasmosis in an immunocompetent patient from a nonendemic region. This finding may expand understanding of histoplasmosis presentations and inform clinical approaches.

gastric involvement with disseminated histoplasmosis in an immunocompetent patient from a nonendemic region

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Gastric Involvement With Disseminated Histoplasmosis in an Immunocompetent Patient From a Nonendemic Region.”

chorea-acanthocytosis parkinsonism-dystonia, infantile+1 moreResearch

Recent research highlights a unique presentation of chorea-acanthocytosis, where VPS13A mutations manifest primarily as parkinsonism rather than chorea. This finding may shift the understanding of the disease's clinical spectrum.

chorea acanthocytosis without chorea vps13a disease manifesting as parkinsonism

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Chorea-Acanthocytosis Without Chorea: VPS13A Disease Manifesting as Parkinsonism.”

collagen type III glomerulopathyResearch

A recent study reports two adult cases of Type III collagen glomerulopathy, highlighting divergent histopathological patterns and potential diagnostic pitfalls. This research contributes to the understanding of this rare kidney disease.

type iii collagen glomerulopathy presenting with divergent histopathological patterns report of two adult cases and diagnostic pitfalls

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Type III Collagen Glomerulopathy Presenting With Divergent Histopathological Patterns: Report of Two Adult Cases and Diagnostic Pitfalls.”

Erdheim-Chester diseaseResearch

A case report highlights the successful treatment of adult-onset central nervous system Erdheim-Chester disease using cladribine and cytarabine. This literature review adds to the understanding of therapeutic options for this rare condition.

adult onset central nervous system erdheim chester disease successfully treated with cladribine and cytarabine case report and literature review

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Adult-Onset Central Nervous System Erdheim-Chester Disease Successfully Treated With Cladribine and Cytarabine: Case Report and Literature Review.”

Duchenne muscular dystrophy DMD-related muscular dystrophyResearch

A recent study highlights the prevalence of adrenal insufficiency in patients with Duchenne muscular dystrophy who are treated with glucocorticoids. The research discusses historical insights, current challenges, and future directions for managing this condition.

adrenal insufficiency in individuals with duchenne muscular dystrophy treated with glucocorticoids insights from the past current challenges and future directions

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Adrenal insufficiency in individuals with Duchenne muscular dystrophy treated with glucocorticoids: Insights from the past, current challenges, and future directions.”

vitiligoResearch

A bibliometric analysis highlights emerging trends in JAK inhibitor therapy for vitiligo from 2015 to 2025. This research identifies key hotspots in the field, indicating a growing interest in targeted treatments for this skin condition.

hotspots and emerging trends in jak inhibitor therapy for vitiligo a bibliometric analysis 2015 2025

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Hotspots and Emerging Trends in JAK Inhibitor Therapy for Vitiligo: A Bibliometric Analysis (2015-2025).”

Graves disease agranulocytosis+1 moreResearch

A recent case study highlights a 12-year-old girl with Graves disease who developed agranulocytosis and thrombocytopenia. This case underscores the potential complications associated with Graves disease in pediatric patients.

graves disease complicated by agranulocytosis and thrombocytopenia in a 12 year old girl

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Graves disease complicated by agranulocytosis and thrombocytopenia in a 12-year-old girl.”

fetal and neonatal alloimmune thrombocytopeniaResearch

A qualitative study explores the lived experiences of patients with fetal and neonatal alloimmune thrombocytopenia, providing insights into their challenges and needs. This research contributes to understanding the impact of the disease on affected families.

understanding the lived experience of fetal and neonatal alloimmune thrombocytopenia a qualitative study

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Understanding the Lived Experience of Fetal and Neonatal Alloimmune Thrombocytopenia: A Qualitative Study.”

Research

A case analysis highlights neonatal acute liver failure potentially linked to gestational alloimmune liver disease. This research contributes to understanding the complexities of liver conditions in newborns.

case analysis of neonatal acute liver failure presumably caused by gestational alloimmune liver disease

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Case Analysis of Neonatal Acute Liver Failure Presumably Caused by Gestational Alloimmune Liver Disease.”

Research

A recent study published in PubMed highlights the rapid disease progression of primary orbital eccrine porocarcinoma using serial [(18)F]FDG PET/CT imaging. This research provides valuable insights into the disease's behavior and potential monitoring strategies.

primary orbital eccrine porocarcinoma serial 18 f fdg pet ct demonstration of rapid disease progression

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Primary Orbital Eccrine Porocarcinoma: Serial [(18)F]FDG PET/CT Demonstration of Rapid Disease Progression.”

Research

A new study identifies predictive factors for malignancy in thyroid nodules among children and adolescents, enhancing diagnostic accuracy. This research could inform clinical decision-making and improve patient outcomes in this demographic.

predictive factors for malignancy of thyroid nodules in children and adolescents

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Predictive Factors for Malignancy of Thyroid Nodules in Children and Adolescents.”

maligant granulosa cell tumor of ovary ovarian granulosa cell tumor+1 moreResearch

A recent study explores the use of docetaxel for recurrent adult granulosa cell tumor, highlighting its potential to enable tertiary cytoreduction. This research contributes to the understanding of treatment options for this rare tumor type.

docetaxel for recurrent adult granulosa cell tumor enabling tertiary cytoreduction

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Docetaxel for recurrent adult granulosa cell tumor enabling tertiary cytoreduction.”

Netherton syndromeResearch

A recent publication details two case reports of dupilumab use in pediatric patients with Netherton syndrome, contributing to the understanding of treatment options for this rare condition. The review of literature highlights the potential benefits and challenges of using dupilumab in this patient population.

dupilumab in paediatric netherton syndrome two case reports and a review of the literature

PubMed Rare Disease·about 1 month ago·Read at source →

Original title: “Dupilumab in Paediatric Netherton Syndrome: Two Case Reports and a Review of the Literature.”

Previous82 / 482Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A case report highlights the delayed diagnosis of tumor-induced osteomalacia due to overlooked hypophosphatemia linked to excess fibroblast growth factor 23. This underscores the need for increased awareness and diagnostic vigilance in similar cases.

A recent case series published in PubMed highlights instances of spontaneous regression in vitreoretinal lymphoma lesions, contributing to the understanding of this rare condition. The findings may influence future research and treatment approaches for lymphoma.

Recent research identifies FAN1 mutations as a contributing factor to karyomegalic nephropathy in chronic kidney disease. This discovery may open new avenues for understanding the genetic basis of kidney disorders.

A recent study highlights pulmonary AL amyloidosis as a significant cause of interstitial lung disease, diagnosed through transbronchial lung biopsy. This discovery may enhance diagnostic accuracy and treatment approaches for affected patients.

A new study identifies immunohistochemical predictors for head and neck mucosal melanoma, potentially aiding in diagnosis and treatment strategies. This research contributes to the understanding of biomarkers in this rare cancer type.

A new German S3-level guideline has been published for the diagnosis and management of rare dental disorders. This guideline aims to standardize care and improve outcomes for patients with these conditions.

A recent study highlights the diagnostic challenges of PTHrP-mediated hypercalcemia in metastatic adrenocortical carcinoma, which can mimic pheochromocytoma. This research underscores the need for careful differentiation in clinical settings.

A case study highlights gastric involvement in disseminated histoplasmosis in an immunocompetent patient from a nonendemic region. This finding may expand understanding of histoplasmosis presentations and inform clinical approaches.

Recent research highlights a unique presentation of chorea-acanthocytosis, where VPS13A mutations manifest primarily as parkinsonism rather than chorea. This finding may shift the understanding of the disease's clinical spectrum.

A recent study reports two adult cases of Type III collagen glomerulopathy, highlighting divergent histopathological patterns and potential diagnostic pitfalls. This research contributes to the understanding of this rare kidney disease.

A case report highlights the successful treatment of adult-onset central nervous system Erdheim-Chester disease using cladribine and cytarabine. This literature review adds to the understanding of therapeutic options for this rare condition.

A recent study highlights the prevalence of adrenal insufficiency in patients with Duchenne muscular dystrophy who are treated with glucocorticoids. The research discusses historical insights, current challenges, and future directions for managing this condition.

A bibliometric analysis highlights emerging trends in JAK inhibitor therapy for vitiligo from 2015 to 2025. This research identifies key hotspots in the field, indicating a growing interest in targeted treatments for this skin condition.

A recent case study highlights a 12-year-old girl with Graves disease who developed agranulocytosis and thrombocytopenia. This case underscores the potential complications associated with Graves disease in pediatric patients.

A qualitative study explores the lived experiences of patients with fetal and neonatal alloimmune thrombocytopenia, providing insights into their challenges and needs. This research contributes to understanding the impact of the disease on affected families.

A case analysis highlights neonatal acute liver failure potentially linked to gestational alloimmune liver disease. This research contributes to understanding the complexities of liver conditions in newborns.

A recent study published in PubMed highlights the rapid disease progression of primary orbital eccrine porocarcinoma using serial [(18)F]FDG PET/CT imaging. This research provides valuable insights into the disease's behavior and potential monitoring strategies.

A new study identifies predictive factors for malignancy in thyroid nodules among children and adolescents, enhancing diagnostic accuracy. This research could inform clinical decision-making and improve patient outcomes in this demographic.

A recent study explores the use of docetaxel for recurrent adult granulosa cell tumor, highlighting its potential to enable tertiary cytoreduction. This research contributes to the understanding of treatment options for this rare tumor type.

Not rare diseases news,
news about your rare disease.