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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.

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Research

A new study presents a microdroplet-based high-throughput screening method for identifying antagonistic bacteria that target Vibrio harveyi, a pathogen affecting penaeid shrimp. This research could lead to innovative strategies for managing bacterial infections in aquaculture.

microdroplet based high throughput screening for antagonistic bacteria targeting penaeid shrimp pathogenic vibrio harveyi

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Microdroplet-based high-throughput screening for antagonistic bacteria targeting penaeid shrimp pathogenic Vibrio harveyi.”

mixed phenotype acute leukemia mixed phenotype acute leukemia with t(v;11q23.3)+1 moreResearch

A multi-center case series investigates clinical outcomes and molecular features of CEBPA-mutated mixed phenotype acute leukemia (MPAL). The findings contribute to understanding the disease's biology and potential treatment strategies.

clinical outcomes and molecular features of cebpa mutated mpal a multi center case series

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Clinical outcomes and molecular features of CEBPA-mutated MPAL: a multi-center case series.”

celiac disease celiac disease-epilepsy-cerebral calcification syndromeResearch

A literature review highlights the emergence of celiac disease following autologous stem cell transplantation (ASCT) in multiple myeloma patients. This intersection presents a rare diagnostic challenge for clinicians managing post-transplant complications.

celiac disease emerging after asct in multiple myeloma a rare diagnostic intersection and literature review

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Celiac Disease Emerging After ASCT in Multiple Myeloma: A Rare Diagnostic Intersection and Literature Review.”

Noonan syndrome Noonan syndrome 8Research

A recent study evaluates the molecular genetics and clinical manifestations of patients with LZTR1-associated Noonan syndrome. This retrospective chart review contributes to the understanding of the genetic underpinnings and clinical features of this rare condition.

evaluation of molecular genetics and clinical manifestations in patients with lztr1 associated noonan syndrome a retrospective chart review and review of literature

PubMed Rare Disease·2 months ago·Read at source →

Original title: “The Evaluation of Molecular Genetics and Clinical Manifestations in Patients With LZTR1-Associated Noonan Syndrome: A Retrospective Chart Review and Review of Literature.”

Research

New research suggests that clinically altered brain activity does not resemble typical aged brain activity, which could impact brain-age modeling and biomarker strategies. This finding may influence how researchers approach the identification of biomarkers for age-related diseases.

clinically altered brain activity may not look like aged brain activity implications for brain age modeling and biomarker strategies

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Clinically altered brain activity may not look like aged brain activity: Implications for brain-age modeling and biomarker strategies.”

toxoplasmosis congenital toxoplasmosis+1 moreResearch

A case report highlights acute respiratory failure caused by pulmonary toxoplasmosis in an immunocompetent patient. This study contributes to the understanding of toxoplasmosis and its potential impact on respiratory health.

acute respiratory failure due to pulmonary toxoplasmosis in an immunocompetent patient a case report

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Acute Respiratory Failure due to Pulmonary Toxoplasmosis in an Immunocompetent Patient: A Case Report.”

hemophagocytic lymphohistiocytosis, familial, 6 diffuse large B-cell lymphoma+1 moreResearch

A recent study highlights hemophagocytic lymphohistiocytosis as a potential initial presentation of occult diffuse large B-cell lymphoma, posing significant diagnostic challenges. This finding underscores the need for heightened awareness among clinicians to improve early detection and treatment outcomes.

hemophagocytic lymphohistiocytosis as the initial presentation of occult diffuse large b cell lymphoma a diagnostic challenge

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Hemophagocytic Lymphohistiocytosis As the Initial Presentation of Occult Diffuse Large B-cell Lymphoma: A Diagnostic Challenge.”

essential thrombocythemiaResearch

A recent study highlights Sweet's syndrome as a potential indicator of hematologic progression in patients with essential thrombocythemia. This discovery may enhance understanding of disease evolution and patient management.

cutaneous clue to clonal evolution sweet s syndrome heralding hematologic progression in essential thrombocythemia

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Cutaneous Clue to Clonal Evolution: Sweet's Syndrome Heralding Hematologic Progression in Essential Thrombocythemia.”

colorectal cancerResearch

A multicenter retrospective analysis evaluates the effectiveness and safety of postoperative hemostatic drugs in colorectal cancer patients. The study utilizes inverse probability of treatment weighting to analyze data from a prospectively collected database.

effectiveness and safety of postoperative hemostatic drugs in colorectal cancer a retrospective analysis of a prospectively collected multicenter database using inverse probability of treatment weighting

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Effectiveness and safety of postoperative hemostatic drugs in colorectal cancer: A retrospective analysis of a prospectively collected multicenter database using inverse probability of treatment weighting.”

gastric adenosquamous carcinoma HIV-associated nephropathy+1 moreResearch

A case report details gastric adenosquamous carcinoma exhibiting a pure squamous phenotype in a patient with HIV. This finding may provide insights into the tumor's behavior and its association with HIV.

gastric adenosquamous carcinoma with an apparently pure squamous phenotype on limited biopsy in a patient with hiv a case report

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Gastric adenosquamous carcinoma with an apparently pure squamous phenotype on limited biopsy in a patient with HIV: A case report.”

von Willebrand disease (hereditary or acquired)von Willebrand disease 2Research

A recent study highlights persistent gingival bleeding after dental scaling as a potential diagnostic indicator for von Willebrand disease. This finding could enhance early detection and management of the condition.

persistent gingival bleeding after scaling a diagnostic clue to von willebrand disease

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Persistent Gingival Bleeding After Scaling: A Diagnostic Clue to von Willebrand Disease.”

Research

A recent study published in PubMed examines the long-term outcomes of pediatric patients with unexplained elevated total immunoglobulin E levels. The findings contribute to understanding the implications of elevated IgE in children, although specific outcomes were not detailed.

long term outcomes of paediatric patients with unexplained elevated total immunoglobulin e

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Long-Term Outcomes of Paediatric Patients With Unexplained Elevated Total Immunoglobulin E.”

hypochondroplasiaResearch

The CANOPY HCH-3 study is a phase 3 trial designed to evaluate the efficacy and safety of vosoritide in children with hypochondroplasia. This randomized, double-blind, placebo-controlled study aims to provide critical data on the treatment's impact.

phase 3 randomized double blind placebo controlled multicenter study to evaluate the efficacy and safety of vosoritide in children with hypochondroplasia canopy hch 3 study design

PubMed Rare Disease·2 months ago·Read at source →

Original title: “A phase 3, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of vosoritide in children with hypochondroplasia: CANOPY HCH-3 study design.”

Research

A narrative review discusses the advancements in pharmaceutical 3D printing, highlighting its potential in personalized medicine and super-compounding pharmacies. This technology could revolutionize drug formulation and delivery, enhancing patient-specific therapies.

pharmaceutical 3d printing from personalized medicine to super compounding pharmacies a narrative review

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Pharmaceutical 3D Printing From Personalized Medicine to Super-Compounding Pharmacies: A Narrative Review.”

Research

A recent study published on PubMed details the natural history and treatment outcomes of aggressive angiomyxoma based on a single institution's experience. This research provides valuable insights into the disease's progression and therapeutic responses.

natural history and treatment outcomes in aggressive angiomyxoma a single institution experience

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Natural history and treatment outcomes in aggressive angiomyxoma: A single institution experience.”

acute necrotizing pancreatitisResearch

A study highlights a rare but life-threatening complication of gastroduodenal artery pseudoaneurysm rupture during endoscopic necrosectomy in patients with severe necrotizing pancreatitis. This finding underscores the need for heightened awareness and careful management in such cases.

catastrophic gastroduodenal artery pseudoaneurysm rupture during endoscopic necrosectomy in severe necrotizing pancreatitis a rare life threatening complication

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Catastrophic Gastroduodenal Artery Pseudoaneurysm Rupture During Endoscopic Necrosectomy in Severe Necrotizing Pancreatitis: A Rare Life-Threatening Complication.”

pediatric arterial ischemic strokeResearch

A prospective cohort study investigates serum biomarker dynamics to predict clinical outcomes and hemorrhagic transformation in acute ischemic stroke. The findings may enhance understanding of stroke management and patient prognosis.

serum biomarker dynamics for predicting clinical outcomes and hemorrhagic transformation in acute ischemic stroke a prospective cohort study

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Serum biomarker dynamics for predicting clinical outcomes and hemorrhagic transformation in acute ischemic stroke:A prospective cohort study.”

pediatric high-grade glioma gliomatosis cerebriResearch

A recent study published in PubMed explores diffuse high-grade glioma with a gliomatosis cerebri pattern, which can mimic symmetric white matter disease. This research contributes to the understanding of glioma presentations and may impact diagnostic approaches.

diffuse high grade glioma with gliomatosis cerebri pattern mimicking symmetric white matter disease

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Diffuse high-grade glioma with gliomatosis cerebri pattern mimicking symmetric white matter disease.”

Research

A recent study published in PubMed details a case of multifocal osseous and cutaneous Rosai-Dorfman-Destombes disease, highlighting its presentation as an aggressive intramedullary femoral lesion. This research contributes to the understanding of this rare disease's clinical manifestations.

multifocal osseous and cutaneous rosai dorfman destombes disease presenting as an aggressive intramedullary femoral lesion

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Multifocal osseous and cutaneous Rosai-Dorfman-Destombes disease presenting as an aggressive intramedullary femoral lesion.”

hereditary spastic paraplegia hereditary spastic paraplegia 30+1 moreResearch

A new cellular imaging-based method shows promise as a potential biomarker for SPG4 hereditary spastic paraplegia. This discovery could enhance diagnostic accuracy and monitoring for this rare genetic condition.

validation of a cellular imaging based method as a potential biomarker for spg4 hereditary spastic paraplegia

PubMed Rare Disease·2 months ago·Read at source →

Original title: “Validation of a Cellular Imaging-Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia.”

Previous123 / 482Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A new study presents a microdroplet-based high-throughput screening method for identifying antagonistic bacteria that target Vibrio harveyi, a pathogen affecting penaeid shrimp. This research could lead to innovative strategies for managing bacterial infections in aquaculture.

A multi-center case series investigates clinical outcomes and molecular features of CEBPA-mutated mixed phenotype acute leukemia (MPAL). The findings contribute to understanding the disease's biology and potential treatment strategies.

A literature review highlights the emergence of celiac disease following autologous stem cell transplantation (ASCT) in multiple myeloma patients. This intersection presents a rare diagnostic challenge for clinicians managing post-transplant complications.

A recent study evaluates the molecular genetics and clinical manifestations of patients with LZTR1-associated Noonan syndrome. This retrospective chart review contributes to the understanding of the genetic underpinnings and clinical features of this rare condition.

New research suggests that clinically altered brain activity does not resemble typical aged brain activity, which could impact brain-age modeling and biomarker strategies. This finding may influence how researchers approach the identification of biomarkers for age-related diseases.

A case report highlights acute respiratory failure caused by pulmonary toxoplasmosis in an immunocompetent patient. This study contributes to the understanding of toxoplasmosis and its potential impact on respiratory health.

A recent study highlights Sweet's syndrome as a potential indicator of hematologic progression in patients with essential thrombocythemia. This discovery may enhance understanding of disease evolution and patient management.

A multicenter retrospective analysis evaluates the effectiveness and safety of postoperative hemostatic drugs in colorectal cancer patients. The study utilizes inverse probability of treatment weighting to analyze data from a prospectively collected database.

A case report details gastric adenosquamous carcinoma exhibiting a pure squamous phenotype in a patient with HIV. This finding may provide insights into the tumor's behavior and its association with HIV.

A recent study highlights persistent gingival bleeding after dental scaling as a potential diagnostic indicator for von Willebrand disease. This finding could enhance early detection and management of the condition.

A recent study published in PubMed examines the long-term outcomes of pediatric patients with unexplained elevated total immunoglobulin E levels. The findings contribute to understanding the implications of elevated IgE in children, although specific outcomes were not detailed.

The CANOPY HCH-3 study is a phase 3 trial designed to evaluate the efficacy and safety of vosoritide in children with hypochondroplasia. This randomized, double-blind, placebo-controlled study aims to provide critical data on the treatment's impact.

A narrative review discusses the advancements in pharmaceutical 3D printing, highlighting its potential in personalized medicine and super-compounding pharmacies. This technology could revolutionize drug formulation and delivery, enhancing patient-specific therapies.

A recent study published on PubMed details the natural history and treatment outcomes of aggressive angiomyxoma based on a single institution's experience. This research provides valuable insights into the disease's progression and therapeutic responses.

A study highlights a rare but life-threatening complication of gastroduodenal artery pseudoaneurysm rupture during endoscopic necrosectomy in patients with severe necrotizing pancreatitis. This finding underscores the need for heightened awareness and careful management in such cases.

A prospective cohort study investigates serum biomarker dynamics to predict clinical outcomes and hemorrhagic transformation in acute ischemic stroke. The findings may enhance understanding of stroke management and patient prognosis.

A recent study published in PubMed explores diffuse high-grade glioma with a gliomatosis cerebri pattern, which can mimic symmetric white matter disease. This research contributes to the understanding of glioma presentations and may impact diagnostic approaches.

A recent study published in PubMed details a case of multifocal osseous and cutaneous Rosai-Dorfman-Destombes disease, highlighting its presentation as an aggressive intramedullary femoral lesion. This research contributes to the understanding of this rare disease's clinical manifestations.

A new cellular imaging-based method shows promise as a potential biomarker for SPG4 hereditary spastic paraplegia. This discovery could enhance diagnostic accuracy and monitoring for this rare genetic condition.

Not rare diseases news,
news about your rare disease.