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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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prostate cancer prostate cancer, hereditary+1 moreResearch

A study published in PubMed explores the transcriptional profiling of circulating extracellular vesicles in prebiopsy prostate cancer patients. This research may provide insights into the molecular characteristics of prostate cancer, potentially aiding in early detection and personalized treatment strategies.

transcriptional profiling of circulating extracellular vesicles from prebiopsy prostate cancer patients

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Transcriptional profiling of circulating extracellular vesicles from prebiopsy prostate cancer patients.”

Research

A study published on PubMed details intestinal entamoebiasis in a captive colony of Anderson's crocodile newts, Echinotriton andersoni. This research contributes to understanding disease impacts in amphibian populations.

intestinal entamoebiasis in a captive colony of anderson s crocodile newts echinotriton andersoni

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Intestinal entamoebiasis in a captive colony of Anderson's crocodile newts Echinotriton andersoni.”

Research

A new study investigates transmission pathways during high-contact care activities in nursing homes using high-fidelity simulations. The findings could inform infection control practices in these settings, although specific disease implications were not detailed.

transmission pathways during high contact care activities in nursing homes a high fidelity simulation study with surrogate markers

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Transmission pathways during high-contact care activities in nursing homes: a high-fidelity simulation study with surrogate markers.”

Research

A case study highlights the diagnostic challenges and successful treatment of severe pulmonary Mycobacterium genavense infection in an immunocompetent adult using a macrolide-based combination therapy. This research underscores the complexities of diagnosing rare mycobacterial infections.

severe pulmonary mycobacterium genavense infection in an immunocompetent adult diagnostic challenges and successful macrolide based combination therapy

PubMed Rare Disease·8 months ago·Read at source →

Original title: “[Severe pulmonary Mycobacterium genavense infection in an immunocompetent adult : Diagnostic challenges and successful macrolide-based combination therapy].”

rhabdoid tumor rhabdoid tumor of the kidney+1 moreResearch

A new report from the Pediatric Surgical Oncology Research Collaborative details outcomes and surgical management strategies for malignant rhabdoid tumor of the kidney. This research provides insights into treatment approaches for this rare pediatric cancer.

outcomes and surgical management of malignant rhabdoid tumor of the kidney a report from the pediatric surgical oncology research collaborative

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Outcomes and Surgical Management of Malignant Rhabdoid Tumor of the Kidney: A Report From the Pediatric Surgical Oncology Research Collaborative.”

multifocal motor neuropathyResearch

A case report highlights multifocal motor neuropathy as a potential secondary condition to gluten intolerance. This finding may prompt further research into the relationship between gluten sensitivity and neurological disorders.

multifocal motor neuropathy secondary to gluten intolerance a case report

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Multifocal motor neuropathy secondary to gluten intolerance: a case report.”

hepatopulmonary syndrome panhypopituitarism+1 moreResearch

A recent study highlights the successful use of growth hormone (GH) treatment for hepatopulmonary syndrome in patients with panhypopituitarism-related advanced liver disease. This research could pave the way for new therapeutic approaches in managing this complex condition.

successful gh treatment of hepatopulmonary syndrome in panhypopituitarism related advanced liver disease

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Successful GH Treatment of Hepatopulmonary Syndrome in Panhypopituitarism-related Advanced Liver Disease.”

congenital primary aphakiaResearch

A recent study investigates the effectiveness of posterior optic capture in pediatric aphakia, suggesting that additional surgical effort may yield better visual outcomes. The findings contribute to the ongoing research in pediatric ophthalmology.

posterior optic capture in pediatric aphakia does extra work pay off

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Posterior optic capture in pediatric aphakia: Does extra work pay off?”

Research

A recent study published in PubMed details the clinicopathological features of extra-appendiceal goblet cell adenocarcinoma, focusing on tumors in the gastrointestinal tract and bile duct. This research contributes to the understanding of this rare cancer type.

extra appendiceal goblet cell adenocarcinoma clinicopathological features of a series of tumors in the gastrointestinal tract and bile duct

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Extra-Appendiceal Goblet Cell Adenocarcinoma: Clinicopathological Features of a Series of Tumors in the Gastrointestinal Tract and Bile Duct.”

Duchenne muscular dystrophy DMD-related muscular dystrophyResearch

A recent cost-utility analysis evaluates the treatment of Ataluren combined with standard care versus standard care alone for patients with Duchenne muscular dystrophy in Brazil. This study provides insights into the economic implications of incorporating Ataluren in treatment regimens.

cost utility analysis of the treatment with ataluren plus standard of care compared with standard of care alone in patients with duchenne muscular dystrophy in brazil

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Cost-Utility Analysis of the Treatment With Ataluren Plus Standard of Care Compared With Standard of Care Alone in Patients With Duchenne Muscular Dystrophy in Brazil.”

Research

A recent study analyzes four cases of intratesticular serous borderline tumors, providing valuable clinicopathologic and molecular insights. This research contributes to the understanding of this rare tumor type, although further studies are needed to establish broader implications.

intratesticular serous borderline tumor a clinicopathologic and molecular analysis of four tumors with literature review

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Intratesticular Serous Borderline Tumor: A Clinicopathologic and Molecular Analysis of Four Tumors With Literature Review.”

linear and whorled nevoid hypermelanosisResearch

A multicenter retrospective study analyzed 33 patients with linear and whorled hypermelanosis, contributing to the understanding of this rare skin condition. The findings may help inform future research and clinical approaches.

linear and whorled hypermelanosis a multicentre retrospective cohort of 33 patients

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Linear and whorled hypermelanosis: A multicentre retrospective cohort of 33 patients.”

non-small cell squamous lung carcinoma non-small cell lung carcinoma+1 moreResearch

A case report highlights a patient with a novel PPP1CB-ALK fusion in advanced non-small cell lung cancer (NSCLC) who achieved long-term survival with alectinib treatment. This finding may provide insights into targeted therapies for similar genetic profiles.

patient with novel ppp1cb alk fusion advanced nsclc achieved long survival from alectinib a case report

PubMed Rare Disease·8 months ago·Read at source →

Original title: “A Patient With Novel PPP1CB -ALK Fusion Advanced NSCLC Achieved Long Survival From Alectinib: A Case Report.”

left ventricular noncompaction 5 left ventricular noncompaction 7Research

A recent case series published in PubMed explores surgical management techniques for left ventricular masses, emphasizing ventricular-sparing approaches. This research contributes to the understanding of cardiac surgery options for rare cardiac conditions.

surgical management of left ventricular masses a case series highlighting ventricular sparing approaches

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Surgical management of left ventricular masses: a case series highlighting ventricular-sparing approaches.”

Research

Beam Therapeutics reports positive data from a small study on its base editing treatment for alpha-1 antitrypsin deficiency (AATD), demonstrating restoration of functional protective proteins. This advancement highlights the potential of gene editing in addressing rare lung and liver conditions.

Updated data showed the biotech's approach to the rare lung and liver condition helped restore functional protective proteins in a small study.

BioPharma Dive·8 months ago·Read at source →

Original title: “Beam posts positive data on base editing treatment for AATD”

congenital heart disease heart conduction disease+1 moreResearch

The PVRI-GoDeep initiative establishes a global meta-registry aimed at improving understanding and treatment of heart and lung diseases. This collaborative effort seeks to enhance data sharing and patient outcomes across various conditions.

pvri godeep a global meta registry at the crossroads of heart and lung

PubMed Rare Disease·8 months ago·Read at source →

Original title: “PVRI-GoDeep-A Global Meta-Registry at the Crossroads of Heart and Lung.”

kidney failureResearch

A recent case report details rapidly progressive kidney failure associated with transient non-cystic kidney enlargement, emphasizing the delayed formation of medullary cysts. This study contributes to the understanding of kidney pathology and may inform future research.

rapidly progressive kidney failure with transient non cystic kidney enlargement a case report highlighting delayed medullary cyst formation

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.”

colorectal cancerResearch

A recent NIH-funded study reveals that chronic inflammation can create lasting changes in gut stem cells, potentially increasing the risk of colorectal cancer. The research indicates that these heritable memories of damage can persist for months after the inflammation has resolved.

NIH-funded animal study finds heritable memories of damage persisted in cells months after inflammation ceased.

NIH News·8 months ago·Read at source →

Original title: “Chronic inflammation leaves long-lasting impression on gut stem cells, increasing colorectal cancer risk”

autism spectrum disorder autism spectrum disorder 2+1 moreResearch

Research identifies monoallelic and biallelic KDM5A variants in patients with autism spectrum disorder, suggesting a genetic link that could inform future therapeutic strategies. This discovery enhances understanding of the genetic underpinnings of autism.

monoallelic and biallelic kdm5a variants identified in patients with autism spectrum disorder

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder.”

peripartum cardiomyopathy dilated cardiomyopathy 1Q+1 moreResearch

A new study evaluates women with peripartum or dilated cardiomyopathy and their first-degree relatives, contributing to the understanding of these conditions. The DCM Precision Medicine Study aims to enhance precision medicine approaches for affected families.

evaluation of women with peripartum or dilated cardiomyopathy and their first degree relatives the dcm precision medicine study

PubMed Rare Disease·8 months ago·Read at source →

Original title: “Evaluation of Women With Peripartum or Dilated Cardiomyopathy and Their First-Degree Relatives: The DCM Precision Medicine Study.”

Previous386 / 488Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A study published on PubMed details intestinal entamoebiasis in a captive colony of Anderson's crocodile newts, Echinotriton andersoni. This research contributes to understanding disease impacts in amphibian populations.

A new study investigates transmission pathways during high-contact care activities in nursing homes using high-fidelity simulations. The findings could inform infection control practices in these settings, although specific disease implications were not detailed.

A case study highlights the diagnostic challenges and successful treatment of severe pulmonary Mycobacterium genavense infection in an immunocompetent adult using a macrolide-based combination therapy. This research underscores the complexities of diagnosing rare mycobacterial infections.

A new report from the Pediatric Surgical Oncology Research Collaborative details outcomes and surgical management strategies for malignant rhabdoid tumor of the kidney. This research provides insights into treatment approaches for this rare pediatric cancer.

A case report highlights multifocal motor neuropathy as a potential secondary condition to gluten intolerance. This finding may prompt further research into the relationship between gluten sensitivity and neurological disorders.

A recent study highlights the successful use of growth hormone (GH) treatment for hepatopulmonary syndrome in patients with panhypopituitarism-related advanced liver disease. This research could pave the way for new therapeutic approaches in managing this complex condition.

A recent study investigates the effectiveness of posterior optic capture in pediatric aphakia, suggesting that additional surgical effort may yield better visual outcomes. The findings contribute to the ongoing research in pediatric ophthalmology.

A recent study published in PubMed details the clinicopathological features of extra-appendiceal goblet cell adenocarcinoma, focusing on tumors in the gastrointestinal tract and bile duct. This research contributes to the understanding of this rare cancer type.

A recent cost-utility analysis evaluates the treatment of Ataluren combined with standard care versus standard care alone for patients with Duchenne muscular dystrophy in Brazil. This study provides insights into the economic implications of incorporating Ataluren in treatment regimens.

A recent study analyzes four cases of intratesticular serous borderline tumors, providing valuable clinicopathologic and molecular insights. This research contributes to the understanding of this rare tumor type, although further studies are needed to establish broader implications.

A multicenter retrospective study analyzed 33 patients with linear and whorled hypermelanosis, contributing to the understanding of this rare skin condition. The findings may help inform future research and clinical approaches.

A case report highlights a patient with a novel PPP1CB-ALK fusion in advanced non-small cell lung cancer (NSCLC) who achieved long-term survival with alectinib treatment. This finding may provide insights into targeted therapies for similar genetic profiles.

A recent case series published in PubMed explores surgical management techniques for left ventricular masses, emphasizing ventricular-sparing approaches. This research contributes to the understanding of cardiac surgery options for rare cardiac conditions.

Beam Therapeutics reports positive data from a small study on its base editing treatment for alpha-1 antitrypsin deficiency (AATD), demonstrating restoration of functional protective proteins. This advancement highlights the potential of gene editing in addressing rare lung and liver conditions.

The PVRI-GoDeep initiative establishes a global meta-registry aimed at improving understanding and treatment of heart and lung diseases. This collaborative effort seeks to enhance data sharing and patient outcomes across various conditions.

A recent case report details rapidly progressive kidney failure associated with transient non-cystic kidney enlargement, emphasizing the delayed formation of medullary cysts. This study contributes to the understanding of kidney pathology and may inform future research.

A recent NIH-funded study reveals that chronic inflammation can create lasting changes in gut stem cells, potentially increasing the risk of colorectal cancer. The research indicates that these heritable memories of damage can persist for months after the inflammation has resolved.

Research identifies monoallelic and biallelic KDM5A variants in patients with autism spectrum disorder, suggesting a genetic link that could inform future therapeutic strategies. This discovery enhances understanding of the genetic underpinnings of autism.

A new study evaluates women with peripartum or dilated cardiomyopathy and their first-degree relatives, contributing to the understanding of these conditions. The DCM Precision Medicine Study aims to enhance precision medicine approaches for affected families.

Not rare diseases news,
news about your rare disease.