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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 study highlights the emergence and transmission of carbapenem-resistant Klebsiella pneumoniae with the bla(NDM-21) gene in a neonatal intensive care unit. This finding raises concerns about antibiotic resistance in vulnerable populations.

emerging infection and nosocomial transmission of carbapenem resistant klebsiella pneumoniae harboring bla ndm 21 in a neonatal intensive care unit

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Emerging infection and nosocomial transmission of carbapenem-resistant Klebsiella pneumoniae harboring bla(NDM-21) in a neonatal intensive care unit.”

rareResearch

A new consensus has been established for next-generation sequencing-based genetic testing in rare neurological diseases. These recommendations aim to enhance diagnostic accuracy and patient management in this challenging field.

consensus recommendations for next generation sequencing based genetic testing in rare neurological diseases

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.”

adenocarcinoma adenocarcinoma in situ+1 moreResearch

A recent publication discusses the complexities faced by surgeons when dealing with subhepatic retained appendiceal tips that harbor adenocarcinoma. This case highlights the challenges in diagnosis and management of rare surgical conditions.

subhepatic retained appendiceal tip harbouring adenocarcinoma a surgeon s dilemma

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Subhepatic retained appendiceal tip harbouring adenocarcinoma: a surgeon's dilemma.”

well-differentiated fetal adenocarcinoma of the lung fetal lung interstitial tumorResearch

A recent literature review highlights a rare case of early-stage high-grade fetal lung adenocarcinoma associated with a KRAS mutation. This discovery adds to the understanding of the genetic factors involved in this uncommon cancer type.

early stage high grade fetal lung adenocarcinoma with kras mutation a rare presentation and literature review

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Early-Stage High-Grade Fetal Lung Adenocarcinoma With KRAS Mutation: A Rare Presentation and Literature Review.”

interstitial lung disease interstitial lung disease 2Research

A new study highlights the use of artificial intelligence in recognizing patterns of interstitial lung disease on high-resolution computed tomography. This advancement aims to enhance diagnostic accuracy for general radiologists.

artificial intelligence for interstitial lung disease pattern recognition on high resolution computed tomography a step forward for general radiologists

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Artificial intelligence for interstitial lung disease pattern recognition on high-resolution computed tomography: A step forward for general radiologists.”

erythema elevatum diutinumResearch

A new publication discusses erythema elevatum diutinum, a rare skin condition characterized by persistent, raised lesions. This research contributes to the understanding of the disease's pathology and potential treatment options.

erythema elevatum diutinum

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Erythema Elevatum Diutinum.”

myxedema coma myxedemaResearch

A case study highlights nontraumatic acute compartment syndrome in all four extremities as a complication of myxedema coma. This research adds to the understanding of rare disease manifestations and their management.

nontraumatic acute compartment syndrome in all four extremities secondary to myxedema coma

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Nontraumatic acute compartment syndrome in all four extremities secondary to myxedema coma.”

Research

Recent research published in PubMed highlights diffuse plane xanthoma, a rare skin condition characterized by yellowish plaques. The study provides insights into its pathophysiology and potential treatment options.

diffuse plane xanthoma

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Diffuse Plane Xanthoma.”

neurosarcoidosis sarcoidosisResearch

A recent study published in PubMed explores pediatric neurosarcoidosis, highlighting cases with cavernous sinus involvement and internal carotid artery stenosis. This research contributes to the understanding of rare neurological manifestations in children.

pediatric neurosarcoidosis with cavernous sinus involvement and internal carotid artery stenosis

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Pediatric neurosarcoidosis with cavernous sinus involvement and internal carotid artery stenosis.”

anterior segment dysgenesis anterior segment dysgenesis 4+1 moreResearch

A study analyzed 111 patients with bilateral anterior segment dysgenesis, aniridia, microphthalmia, and anophthalmia, providing insights into the molecular and clinical characteristics of these conditions. The findings may enhance understanding and management of these rare eye disorders.

molecular and clinical analyses of 111 patients with bilateral anterior segment dysgenesis aniridia and microphthalmia anophthalmia

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Molecular and Clinical Analyses of 111 Patients with Bilateral Anterior-Segment Dysgenesis/Aniridia and Microphthalmia/Anophthalmia.”

Research

Recent research highlights the associations between cutaneous granulomatous disorders and malignancy, providing insights into potential underlying mechanisms. This study may inform future diagnostic and therapeutic strategies for affected patients.

cutaneous granulomatous disorders and associations with malignancy

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Cutaneous granulomatous disorders and associations with malignancy.”

hypophosphatasia infantile hypophosphatasia+1 moreResearch

A study reports a 17-year follow-up of middle-aged siblings diagnosed with hypophosphatasia, revealing a novel intronic and a rare missense mutation in the ALPL gene. This research contributes to the understanding of genetic factors in hypophosphatasia.

seventeen year follow up of hypophosphatasia diagnosed in middle aged siblings harboring a novel intronic and a rare missense alpl gene mutation

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Seventeen-year follow-up of hypophosphatasia diagnosed in middle-aged siblings harboring a novel intronic and a rare missense ALPL gene mutation.”

visceral leishmaniasis hemophagocytic lymphohistiocytosis, familial, 6Research

A case report highlights the diagnostic challenges of visceral leishmaniasis-associated hemophagocytic lymphohistiocytosis in a patient with Crohn's disease undergoing anti-TNFα therapy. This study underscores the complexities of diagnosing rare diseases in patients with existing conditions.

visceral leishmaniasis associated hemophagocytic lymphohistiocytosis in a patient with crohn s disease in therapy with anti tnf a challenging diagnostic case report

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Visceral Leishmaniasis-Associated Hemophagocytic Lymphohistiocytosis in a Patient With Crohn's Disease in Therapy With Anti-TNFα: A Challenging Diagnostic Case Report.”

Research

India is enhancing its pandemic preparedness through stakeholder consultations at four zonal institutes of virology. These efforts aim to improve outbreak response and establish collaborative research priorities.

strengthening india s pandemic preparedness with the four zonal institutes of virology stakeholder consultations for outbreak response and collaborative research priorities

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Strengthening India's pandemic preparedness with the four zonal institutes of virology: stakeholder consultations for outbreak response and collaborative research priorities.”

type 2 diabetes mellitus maturity-onset diabetes of the young type 2Research

A multicenter retrospective study evaluates the long-term effects of lobeglitazone on renal function and albuminuria in Korean patients with type 2 diabetes mellitus. The findings contribute to understanding the drug's impact on kidney health in this population.

effects of long term lobeglitazone treatment on renal function and albuminuria in korean patients with type 2 diabetes mellitus a multicenter retrospective observational study lucky

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Effects of Long-Term Lobeglitazone Treatment on Renal Function and Albuminuria in Korean Patients with Type 2 Diabetes Mellitus: A Multicenter Retrospective Observational Study (LUCKY).”

bladder squamous cell carcinoma gallbladder squamous cell carcinomaResearch

The French AVENTUR Group presents a comprehensive review of current evidence and therapeutic challenges in squamous cell carcinoma of the bladder. This publication highlights ongoing research perspectives that may inform future treatment strategies.

squamous cell carcinoma of the bladder current evidence therapeutic challenges and research perspectives from the french aventur group

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Squamous Cell Carcinoma of the Bladder: Current Evidence, Therapeutic Challenges, and Research Perspectives from the French AVENTUR Group.”

Research

Research reveals that 10-gingerol mitigates arsenic trioxide-induced cardiotoxicity through mechanisms involving the PI3K/AKT pathway. This study combines network pharmacology with experimental validation, contributing to the understanding of cardiotoxic effects.

10 gingerol alleviates arsenic trioxide induced cardiotoxicity mechanisms involving the pi3k akt pathway revealed by network pharmacology and experimental validation

PubMed Rare Disease·3 months ago·Read at source →

Original title: “10-Gingerol Alleviates Arsenic Trioxide-Induced Cardiotoxicity: Mechanisms Involving the PI3K/AKT Pathway Revealed by Network Pharmacology and Experimental Validation.”

liver disease, severe congenital polycystic liver disease 2+1 moreResearch

A recent study investigates the impact of maternal exposure to particulate matter during pregnancy on offspring liver function. The findings contribute to understanding environmental factors affecting liver health in children.

maternal exposure to particulate matter during pregnancy and offspring liver function

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Maternal exposure to particulate matter during pregnancy and offspring liver function.”

Research

A new study explores how energetic thresholds and hygienic cannibalism influence the founding of claustral ant colonies when faced with fungal challenges. This research provides insights into ant behavior and survival strategies in adverse conditions.

energetic thresholds and hygienic cannibalism govern claustral ant colony founding under fungal challenge

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Energetic thresholds and hygienic cannibalism govern claustral ant colony founding under fungal challenge.”

Research

Research highlights the development of enantiomeric single-atom nanoagents for the treatment of Alzheimer's disease using diazonium-enabled post-synthetic construction. This innovative approach could pave the way for new therapeutic strategies in managing Alzheimer's.

diazonium enabled post synthetic construction of enantiomeric single atom nanoagents used for alzheimer s disease treatment

PubMed Rare Disease·3 months ago·Read at source →

Original title: “Diazonium-Enabled Post-Synthetic Construction of Enantiomeric Single-Atom Nanoagents Used for Alzheimer's Disease Treatment.”

Previous204 / 484Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A study highlights the emergence and transmission of carbapenem-resistant Klebsiella pneumoniae with the bla(NDM-21) gene in a neonatal intensive care unit. This finding raises concerns about antibiotic resistance in vulnerable populations.

A new consensus has been established for next-generation sequencing-based genetic testing in rare neurological diseases. These recommendations aim to enhance diagnostic accuracy and patient management in this challenging field.

A recent publication discusses the complexities faced by surgeons when dealing with subhepatic retained appendiceal tips that harbor adenocarcinoma. This case highlights the challenges in diagnosis and management of rare surgical conditions.

A recent literature review highlights a rare case of early-stage high-grade fetal lung adenocarcinoma associated with a KRAS mutation. This discovery adds to the understanding of the genetic factors involved in this uncommon cancer type.

A new study highlights the use of artificial intelligence in recognizing patterns of interstitial lung disease on high-resolution computed tomography. This advancement aims to enhance diagnostic accuracy for general radiologists.

A new publication discusses erythema elevatum diutinum, a rare skin condition characterized by persistent, raised lesions. This research contributes to the understanding of the disease's pathology and potential treatment options.

A case study highlights nontraumatic acute compartment syndrome in all four extremities as a complication of myxedema coma. This research adds to the understanding of rare disease manifestations and their management.

Recent research published in PubMed highlights diffuse plane xanthoma, a rare skin condition characterized by yellowish plaques. The study provides insights into its pathophysiology and potential treatment options.

A recent study published in PubMed explores pediatric neurosarcoidosis, highlighting cases with cavernous sinus involvement and internal carotid artery stenosis. This research contributes to the understanding of rare neurological manifestations in children.

A study analyzed 111 patients with bilateral anterior segment dysgenesis, aniridia, microphthalmia, and anophthalmia, providing insights into the molecular and clinical characteristics of these conditions. The findings may enhance understanding and management of these rare eye disorders.

Recent research highlights the associations between cutaneous granulomatous disorders and malignancy, providing insights into potential underlying mechanisms. This study may inform future diagnostic and therapeutic strategies for affected patients.

A study reports a 17-year follow-up of middle-aged siblings diagnosed with hypophosphatasia, revealing a novel intronic and a rare missense mutation in the ALPL gene. This research contributes to the understanding of genetic factors in hypophosphatasia.

A case report highlights the diagnostic challenges of visceral leishmaniasis-associated hemophagocytic lymphohistiocytosis in a patient with Crohn's disease undergoing anti-TNFα therapy. This study underscores the complexities of diagnosing rare diseases in patients with existing conditions.

India is enhancing its pandemic preparedness through stakeholder consultations at four zonal institutes of virology. These efforts aim to improve outbreak response and establish collaborative research priorities.

A multicenter retrospective study evaluates the long-term effects of lobeglitazone on renal function and albuminuria in Korean patients with type 2 diabetes mellitus. The findings contribute to understanding the drug's impact on kidney health in this population.

The French AVENTUR Group presents a comprehensive review of current evidence and therapeutic challenges in squamous cell carcinoma of the bladder. This publication highlights ongoing research perspectives that may inform future treatment strategies.

Research reveals that 10-gingerol mitigates arsenic trioxide-induced cardiotoxicity through mechanisms involving the PI3K/AKT pathway. This study combines network pharmacology with experimental validation, contributing to the understanding of cardiotoxic effects.

A recent study investigates the impact of maternal exposure to particulate matter during pregnancy on offspring liver function. The findings contribute to understanding environmental factors affecting liver health in children.

A new study explores how energetic thresholds and hygienic cannibalism influence the founding of claustral ant colonies when faced with fungal challenges. This research provides insights into ant behavior and survival strategies in adverse conditions.

Research highlights the development of enantiomeric single-atom nanoagents for the treatment of Alzheimer's disease using diazonium-enabled post-synthetic construction. This innovative approach could pave the way for new therapeutic strategies in managing Alzheimer's.

Not rare diseases news,
news about your rare disease.