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

drug-induced liver injuryResearch

A case report highlights a possible mixed drug-induced liver injury associated with meropenem, evaluated using the updated RUCAM criteria. This study contributes to understanding the hepatotoxic effects of antibiotics in rare cases.

meropenem induced possible mixed drug induced liver injury with cholestatic evolution a case report evaluated using the updated rucam 2016

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

Original title: “Meropenem-Induced Possible Mixed Drug-Induced Liver Injury With Cholestatic Evolution: A Case Report Evaluated Using the Updated RUCAM (2016).”

xeroderma pigmentosum xeroderma pigmentosum group G+1 moreResearch

A recent study reviews five cases of central nervous system tumors in patients with xeroderma pigmentosum, contributing to the understanding of this rare disease's complications. The findings highlight the need for increased surveillance and research into the mechanisms linking xeroderma pigmentosum and tumor development.

central nervous system tumors in xeroderma pigmentosum five cases and review of the literature

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

Original title: “Central Nervous System Tumors in Xeroderma Pigmentosum: Five Cases and Review of the Literature.”

Research

A recent study published in PubMed examines mortality and survival rates associated with Addison's disease in Italy, highlighting the impact of different etiologies. This research contributes to understanding patient outcomes and may inform future treatment approaches.

addison s disease in italy mortality and survival by etiology

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

Original title: “Addison's disease in Italy: mortality and survival by etiology.”

autism autism spectrum disorderResearch

Research indicates that disruption of the MSL2 gene is linked to autism-like behaviors and negatively impacts neurogenesis. The study also highlights alterations in histone H4K16 acetylation, suggesting potential epigenetic mechanisms involved in autism.

msl2 disruption leads to autism like behaviors impairs neurogenesis and alters histone h4k16 acetylation

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

Original title: “MSL2 disruption leads to autism-like behaviors, impairs neurogenesis, and alters histone H4K16 acetylation.”

myeloid sarcomaResearch

A case report highlights a rare instance of primary isolated lumbar spine myeloid sarcoma, contributing to the limited literature on this condition. The findings may inform future research and clinical approaches to similar rare cases.

primary isolated lumbar spine myeloid sarcoma a rare case report and review of the literature

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

Original title: “Primary isolated lumbar spine myeloid sarcoma: a rare case report and review of the literature.”

congenital hypothyroidismResearch

A new publication discusses the genetics and management strategies for congenital hypothyroidism, providing insights into patient care. This research highlights the importance of early diagnosis and intervention in improving patient outcomes.

approach to the patient genetics and management of congenital hypothyroidism

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

Original title: “APPROACH TO THE PATIENT: Genetics and Management of Congenital Hypothyroidism.”

Research

A national study identifies the uric acid to HDL-C ratio as a potential novel biomarker for sarcopenia, utilizing machine learning techniques. This research could pave the way for improved diagnostics and management strategies for sarcopenia.

uric acid to hdl c ratio as a novel biomarker for sarcopenia a national study with machine learning insights

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

Original title: “Uric Acid to HDL-C Ratio as a Novel Biomarker for Sarcopenia: A National Study with Machine Learning Insights.”

Research

A new study introduces SHIELD, a weakly supervised graph attention neural network designed to decode disease-relevant cell-cell interactions. This innovative approach could enhance understanding of cellular mechanisms in various diseases.

shield a weakly supervised graph attention neural network for decoding disease relevant cell cell interactions

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

Original title: “SHIELD: A weakly supervised graph attention neural network for decoding disease-relevant cell-cell interactions.”

colorectal cancerResearch

A rare case report details synchronous isolated cystic pancreatic metastasis originating from primary colorectal cancer. This discovery adds to the understanding of metastatic patterns in colorectal cancer.

synchronous isolated cystic pancreatic metastasis arising from primary colorectal cancer a rare case report

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

Original title: “Synchronous Isolated Cystic Pancreatic Metastasis Arising From Primary Colorectal Cancer: A Rare Case Report.”

rhabdomyosarcomaResearch

Research indicates that high levels of dynein negatively affect mitochondrial distribution and differentiation in rhabdomyosarcoma cells. This study provides insights into the cellular mechanisms that could influence treatment strategies for this rare cancer.

high level dynein impairs mitochondrial distribution and differentiation of rhabdomyosarcoma cells

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

Original title: “High level dynein impairs mitochondrial distribution and differentiation of rhabdomyosarcoma cells.”

Research

A recent study highlights the prevalence of protocadherin 7 positive membranous nephropathy in China, contributing to the understanding of this rare kidney disease. The findings may inform future research and treatment strategies.

protocadherin 7 positive membranous nephropathy in china

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

Original title: “Protocadherin 7 Positive Membranous Nephropathy in China.”

Research

Invalid nucleic acid test results could significantly restrict the use of organs from deceased donors, impacting transplant outcomes. This highlights the need for improved testing methods to enhance organ availability.

invalid nucleic acid test results may limit deceased donor organ utilization

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

Original title: “Invalid Nucleic Acid Test Results May Limit Deceased Donor Organ Utilization.”

Larsen syndrome Reunion island Larsen syndromeResearch

A recent study expands the understanding of GZF1-related phenotype, identifying it as a distinct ocular and skeletal disorder separate from Larsen syndrome. This research enhances the genetic and clinical knowledge surrounding these conditions.

expanding the genetic and clinical spectrum of gzf1 related phenotype a specific ocular and skeletal disorder distinguishable from larsen syndrome

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

Original title: “Expanding the Genetic and Clinical Spectrum of GZF1-Related Phenotype: A Specific Ocular and Skeletal Disorder Distinguishable From Larsen Syndrome.”

paraganglioma pheochromocytoma/paraganglioma syndrome 5+1 moreResearch

A recent study investigates the necessity of preoperative adrenoceptor blockade in patients with paraganglioma. The findings contribute to the ongoing discussion regarding optimal management strategies for this rare tumor.

is preoperative adrenoceptor blockade necessary in patients with paraganglioma

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

Original title: “Is preoperative adrenoceptor blockade necessary in patients with paraganglioma?”

episodic kinesigenic dyskinesia 1 episodic kinesigenic dyskinesiaResearch

A clinical report details 10 cases of paroxysmal kinesigenic dyskinesia from three pedigrees, contributing to the understanding of this rare movement disorder. The study includes a literature review that may inform future research and clinical approaches.

paroxysmal kinesigenic dyskinesia clinical report of 10 cases from three pedigrees with literature review

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

Original title: “Paroxysmal kinesigenic dyskinesia: clinical report of 10 cases from three pedigrees with literature review.”

thalassemia beta-thalassemia HBB/LCRBResearch

A new study presents a prospective multi-center newborn screening for thalassemia using comprehensive analysis of thalassemia alleles through single molecule real-time sequencing in Guangxi, China. This research aims to enhance early detection and management of thalassemia in newborns.

prospective multi center newborn screening for thalassemia by comprehensive analysis of thalassemia alleles catsa based on single molecule real time sequencing in guangxi china

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

Original title: “A Prospective Multi-Center Newborn Screening for Thalassemia by Comprehensive Analysis of Thalassemia Alleles (CATSA) Based on Single Molecule Real-Time Sequencing in Guangxi, China.”

demyelinating diseaseResearch

Recent research highlights advances in imaging techniques for demyelinating and dysmyelinating white matter lesions, potentially improving diagnosis and monitoring of related conditions. These developments could enhance understanding of diseases affecting myelin integrity.

recent advances in imaging of demyelinating and dysmyelinating white matter lesions

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

Original title: “Recent Advances in Imaging of Demyelinating and Dysmyelinating White Matter Lesions.”

Research

A new publication discusses the ethical and normative considerations surrounding genome-wide screening. The study emphasizes the importance of stakeholder engagement in developing responsible screening practices.

towards responsible genome wide screening normative and stakeholder considerations

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

Original title: “Towards responsible genome-wide screening: normative and stakeholder considerations.”

Research

A new publication explores the JNK signaling pathway's role in drug addiction, providing insights into potential therapeutic targets. This research could inform future studies aimed at addressing addiction mechanisms.

mechanism of the jnk signaling pathway in drug addiction author list

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

Original title: “The mechanism of the JNK signaling pathway in drug addiction : Author list.”

psoriatic arthritis herpes zoster+1 moreResearch

A case report highlights that treatment with the AstraZeneca vaccine post-COVID-19 exacerbated arthritis and increased susceptibility to herpes in an older woman. This finding may prompt further investigation into vaccine effects on pre-existing conditions.

post covid 19 treated with astrazeneca vaccine exacerbates arthritis with susceptibility to herpes in an older woman a case report

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

Original title: “Post COVID-19 treated with AstraZeneca vaccine exacerbates arthritis with susceptibility to herpes in an older woman: A case report.”

Previous287 / 486Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A case report highlights a possible mixed drug-induced liver injury associated with meropenem, evaluated using the updated RUCAM criteria. This study contributes to understanding the hepatotoxic effects of antibiotics in rare cases.

A recent study published in PubMed examines mortality and survival rates associated with Addison's disease in Italy, highlighting the impact of different etiologies. This research contributes to understanding patient outcomes and may inform future treatment approaches.

Research indicates that disruption of the MSL2 gene is linked to autism-like behaviors and negatively impacts neurogenesis. The study also highlights alterations in histone H4K16 acetylation, suggesting potential epigenetic mechanisms involved in autism.

A case report highlights a rare instance of primary isolated lumbar spine myeloid sarcoma, contributing to the limited literature on this condition. The findings may inform future research and clinical approaches to similar rare cases.

A new publication discusses the genetics and management strategies for congenital hypothyroidism, providing insights into patient care. This research highlights the importance of early diagnosis and intervention in improving patient outcomes.

A national study identifies the uric acid to HDL-C ratio as a potential novel biomarker for sarcopenia, utilizing machine learning techniques. This research could pave the way for improved diagnostics and management strategies for sarcopenia.

A new study introduces SHIELD, a weakly supervised graph attention neural network designed to decode disease-relevant cell-cell interactions. This innovative approach could enhance understanding of cellular mechanisms in various diseases.

A rare case report details synchronous isolated cystic pancreatic metastasis originating from primary colorectal cancer. This discovery adds to the understanding of metastatic patterns in colorectal cancer.

Research indicates that high levels of dynein negatively affect mitochondrial distribution and differentiation in rhabdomyosarcoma cells. This study provides insights into the cellular mechanisms that could influence treatment strategies for this rare cancer.

A recent study highlights the prevalence of protocadherin 7 positive membranous nephropathy in China, contributing to the understanding of this rare kidney disease. The findings may inform future research and treatment strategies.

Invalid nucleic acid test results could significantly restrict the use of organs from deceased donors, impacting transplant outcomes. This highlights the need for improved testing methods to enhance organ availability.

A recent study expands the understanding of GZF1-related phenotype, identifying it as a distinct ocular and skeletal disorder separate from Larsen syndrome. This research enhances the genetic and clinical knowledge surrounding these conditions.

A recent study investigates the necessity of preoperative adrenoceptor blockade in patients with paraganglioma. The findings contribute to the ongoing discussion regarding optimal management strategies for this rare tumor.

A clinical report details 10 cases of paroxysmal kinesigenic dyskinesia from three pedigrees, contributing to the understanding of this rare movement disorder. The study includes a literature review that may inform future research and clinical approaches.

A new study presents a prospective multi-center newborn screening for thalassemia using comprehensive analysis of thalassemia alleles through single molecule real-time sequencing in Guangxi, China. This research aims to enhance early detection and management of thalassemia in newborns.

Recent research highlights advances in imaging techniques for demyelinating and dysmyelinating white matter lesions, potentially improving diagnosis and monitoring of related conditions. These developments could enhance understanding of diseases affecting myelin integrity.

A new publication discusses the ethical and normative considerations surrounding genome-wide screening. The study emphasizes the importance of stakeholder engagement in developing responsible screening practices.

A new publication explores the JNK signaling pathway's role in drug addiction, providing insights into potential therapeutic targets. This research could inform future studies aimed at addressing addiction mechanisms.

A case report highlights that treatment with the AstraZeneca vaccine post-COVID-19 exacerbated arthritis and increased susceptibility to herpes in an older woman. This finding may prompt further investigation into vaccine effects on pre-existing conditions.

Not rare diseases news,
news about your rare disease.