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What's new in your rare disease | Kisho

Not rare diseases news,
news about your rare disease.

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Research

A rare case study details a cutaneous infection caused by Corynascus verrucosus in a Shih Tzu dog, highlighting molecular identification and phylogenetic analysis. This research contributes to the understanding of rare fungal infections in veterinary medicine.

rare case of cutaneous infection by corynascus verrucosus in a shih tzu dog molecular identification and phylogenetic analysis

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

Original title: “A Rare Case of Cutaneous Infection by Corynascus verrucosus in a Shih Tzu Dog: Molecular Identification and Phylogenetic Analysis.”

Fitz-Hugh-Curtis syndromeResearch

A rare case study highlights the association of cholecystogastric fistula with transient gallstone ileus and incidental Fitz-Hugh-Curtis syndrome. This unique presentation underscores the complexity of diagnosing and managing rare gastrointestinal conditions.

cholecystogastric fistula presenting with transient gallstone ileus and incidental fitz hugh curtis syndrome a rare radiological and intraoperative association

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

Original title: “Cholecystogastric fistula presenting with transient gallstone ileus and incidental Fitz-Hugh-Curtis syndrome: A rare radiological and intraoperative association.”

Research

A recent publication details two cases of primary renal neuroendocrine tumors presenting as complex cystic masses in patients with horseshoe kidneys. This research contributes to the understanding of rare tumor presentations and their implications for diagnosis and treatment.

primary renal neuroendocrine tumors presenting as a complex cystic mass and arising in a horseshoe kidney a report of two cases

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

Original title: “Primary Renal Neuroendocrine Tumors Presenting as a Complex Cystic Mass and Arising in a Horseshoe Kidney: A Report of Two Cases.”

light chain deposition diseaseResearch

The CARES clinical trials provide insights into the effects of anselamimab on cardiac structure and function in patients with light chain amyloidosis. This research highlights potential therapeutic benefits for a condition that significantly impacts heart health.

effect of anselamimab on cardiac structure and function in patients with light chain amyloidosis insights from the cares clinical trials

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

Original title: “Effect of Anselamimab on Cardiac Structure and Function in Patients With Light Chain Amyloidosis: Insights From the CARES Clinical Trials.”

diabetes mellitusResearch

A case report highlights the development of unilateral Graves' disease in a patient undergoing treatment with tirzepatide for diabetes. This finding may prompt further investigation into the potential autoimmune effects of tirzepatide.

unilateral graves disease developing during treatment with tirzepatide in a patient with diabetes a case report

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

Original title: “Unilateral Graves' Disease Developing During Treatment With Tirzepatide in a Patient With Diabetes: A Case Report.”

systemic lupus erythematosus systemic lupus erythematosus related to C1QA+1 moreResearch

New research highlights the role of abnormal copper metabolism in systemic lupus erythematosus, suggesting potential pathways for therapeutic intervention. This study adds to the understanding of the disease's underlying mechanisms.

unveiling the role of abnormal copper metabolism in systemic lupus erythematosus

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

Original title: “Unveiling the role of abnormal copper metabolism in systemic lupus erythematosus.”

leprosy uveitis+1 moreResearch

A study published on PubMed examines the clinical profile of uveitis in leprosy patients in Egypt, providing insights into the ocular complications associated with the disease. This research contributes to the understanding of leprosy-related conditions and their management.

clinical profile of uveitis in leprosy in a cohort of patients in egypt

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

Original title: “Clinical profile of uveitis in leprosy in a cohort of patients in Egypt.”

streptococcal toxic-shock syndromeResearch

A recent publication discusses the ongoing diagnostic and therapeutic challenges associated with streptococcal toxic shock syndrome. The study highlights the need for improved strategies to manage this rare but severe condition.

streptococcal toxic shock syndrome persistent diagnostic and therapeutic challenges

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

Original title: “Streptococcal Toxic Shock Syndrome: Persistent Diagnostic and Therapeutic Challenges.”

Research

A recent study identifies concurrent BCR::ABL1 and SET::NUP214 fusions in patients with blast-phase chronic myeloid leukemia. This discovery may provide insights into the molecular mechanisms underlying this aggressive form of leukemia.

concurrent bcr abl1 and set nup214 fusions in blast phase chronic myeloid leukemia

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

Original title: “Concurrent BCR::ABL1 and SET::NUP214 fusions in blast-phase chronic myeloid leukemia.”

Brugada syndrome Brugada syndrome 7+1 moreResearch

A German multicenter study highlights the diagnostic challenges and clinical outcomes of Brugada syndrome in pediatric patients. The findings underscore the need for improved diagnostic strategies in this rare condition.

brugada syndrome in the pediatric population diagnostic challenges and clinical outcome results of the german multicenter study cogia

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

Original title: “Brugada Syndrome in the Pediatric Population: Diagnostic Challenges and Clinical Outcome-Results of the German Multicenter Study COGIA.”

Research

A multicenter cross-sectional study in Tanzania reveals gaps in knowledge regarding haemophilia care among healthcare providers. This research highlights the need for improved education and training to enhance patient outcomes in this rare disease.

knowledge on the haemophilia care among healthcare providers in tanzania a multicenter cross sectional study

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

Original title: “Knowledge on the Haemophilia Care Among Healthcare Providers in Tanzania: A Multicenter Cross-Sectional Study.”

central nervous system infectious disorder viral infection of central nervous systemResearch

A recent study highlights a case of fatal tension pneumocephalus linked to a central nervous system infection from an extended-spectrum β-lactamase-producing Klebsiella pneumoniae. The research emphasizes the role of hypervirulence-associated genes in this severe infection.

fatal tension pneumocephalus associated with central nervous system infection caused by an extended spectrum lactamase producing klebsiella pneumoniae harboring hypervirulence associated genes

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

Original title: “Fatal Tension Pneumocephalus Associated with Central Nervous System Infection Caused by an Extended-Spectrum β-Lactamase-Producing Klebsiella pneumoniae Harboring Hypervirulence-Associated Genes.”

dysphagia lusoriaResearch

A rare case report details an oropharyngeal leech infestation in a child, leading to epistaxis and dysphagia. This case highlights the unusual presentations of leech infestations in pediatric patients.

rare case of oropharyngeal leech infestation causing epistaxis and dysphagia in a child in herat afghanistan a case report

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

Original title: “A Rare Case of Oropharyngeal Leech Infestation Causing Epistaxis and Dysphagia in a Child in Herat, Afghanistan: A Case Report.”

Research

A recent study published in PubMed examines the incidence of surgical site infections following external ventricular drain placement, identifying key patient-related and periprocedural risk factors. This research contributes to understanding complications in neurosurgery and may inform future clinical practices.

surgical site infections after external ventricular drain placement incidence patient related and periprocedural risk factors

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

Original title: “Surgical Site Infections After External Ventricular Drain Placement: Incidence, Patient-Related, and Periprocedural Risk Factors.”

myelofibrosis tuberculosis+1 moreResearch

A case report highlights myeloid sarcoma as an extramedullary blast crisis in a patient with BCR-ABL1 e6a2+ chronic myeloid leukemia (CML) complicated by myelofibrosis and tuberculosis. This finding may provide insights into the complex interactions between these conditions.

myeloid sarcoma as em blast crisis in bcr abl1 e6a2 cml with myelofibrosis and tb a case report

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

Original title: “Myeloid sarcoma as EM blast crisis in BCR-ABL1 e6a2+ CML with myelofibrosis and TB: a case report.”

Research

A case report highlights the TSHR Gly413Ser mutation's role in familial nonautoimmune hyperthyroidism. This discovery adds to the understanding of genetic factors influencing thyroid disorders.

tshr gly413ser in familial nonautoimmune hyperthyroidism a case report

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

Original title: “TSHR Gly413Ser in familial nonautoimmune hyperthyroidism: a case report.”

primary ciliary dyskinesia primary ciliary dyskinesia 17+1 moreResearch

A recent case-control study investigates the role of hepatocyte growth factor in children with primary ciliary dyskinesia, highlighting its potential relation to disease severity. This research contributes to understanding the biological mechanisms underlying this rare condition.

hepatocyte growth factor in children of primary ciliary dyskinesia and its relation to disease severity a case control study

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

Original title: “Hepatocyte Growth Factor in Children of Primary Ciliary Dyskinesia and Its Relation to Disease Severity. A case-control study.”

thyroid gland papillary carcinoma multicentric papillary thyroid carcinomaResearch

A new study highlights the diffuse sclerosing variant of papillary thyroid carcinoma as a rare and invasive cancer in childhood. This research underscores the challenges in diagnosing and treating this specific cancer variant.

rare invasive and challenging cancer in childhood diffuse sclerosing variant of papillary thyroid carcinoma

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

Original title: “A rare, invasive, and challenging cancer in childhood: diffuse sclerosing variant of papillary thyroid carcinoma.”

pulmonary fibrosisResearch

A study published in PubMed reveals that early fibrotic remodeling in a rat model is responsive to autologous fat grafting. These histological findings could inform future therapeutic strategies for fibrosis-related conditions.

early fibrotic remodeling remains responsive to autologous fat grafting histological findings in a rat model

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

Original title: “Early Fibrotic Remodeling Remains Responsive to Autologous Fat Grafting: Histological Findings in a Rat Model.”

salivary duct carcinoma salivary duct calculiResearch

A recent study published in PubMed evaluates the efficacy of S-1 monotherapy for treating salivary duct carcinoma with MYC amplification. The findings contribute to understanding treatment options for this rare cancer type.

efficacy of s 1 monotherapy for salivary duct carcinoma with myc amplification

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

Original title: “Efficacy of S-1 Monotherapy for Salivary Duct Carcinoma With MYC Amplification.”

Previous130 / 482Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A rare case study details a cutaneous infection caused by Corynascus verrucosus in a Shih Tzu dog, highlighting molecular identification and phylogenetic analysis. This research contributes to the understanding of rare fungal infections in veterinary medicine.

A rare case study highlights the association of cholecystogastric fistula with transient gallstone ileus and incidental Fitz-Hugh-Curtis syndrome. This unique presentation underscores the complexity of diagnosing and managing rare gastrointestinal conditions.

A recent publication details two cases of primary renal neuroendocrine tumors presenting as complex cystic masses in patients with horseshoe kidneys. This research contributes to the understanding of rare tumor presentations and their implications for diagnosis and treatment.

The CARES clinical trials provide insights into the effects of anselamimab on cardiac structure and function in patients with light chain amyloidosis. This research highlights potential therapeutic benefits for a condition that significantly impacts heart health.

A case report highlights the development of unilateral Graves' disease in a patient undergoing treatment with tirzepatide for diabetes. This finding may prompt further investigation into the potential autoimmune effects of tirzepatide.

New research highlights the role of abnormal copper metabolism in systemic lupus erythematosus, suggesting potential pathways for therapeutic intervention. This study adds to the understanding of the disease's underlying mechanisms.

A study published on PubMed examines the clinical profile of uveitis in leprosy patients in Egypt, providing insights into the ocular complications associated with the disease. This research contributes to the understanding of leprosy-related conditions and their management.

A recent publication discusses the ongoing diagnostic and therapeutic challenges associated with streptococcal toxic shock syndrome. The study highlights the need for improved strategies to manage this rare but severe condition.

A recent study identifies concurrent BCR::ABL1 and SET::NUP214 fusions in patients with blast-phase chronic myeloid leukemia. This discovery may provide insights into the molecular mechanisms underlying this aggressive form of leukemia.

A German multicenter study highlights the diagnostic challenges and clinical outcomes of Brugada syndrome in pediatric patients. The findings underscore the need for improved diagnostic strategies in this rare condition.

A multicenter cross-sectional study in Tanzania reveals gaps in knowledge regarding haemophilia care among healthcare providers. This research highlights the need for improved education and training to enhance patient outcomes in this rare disease.

A recent study highlights a case of fatal tension pneumocephalus linked to a central nervous system infection from an extended-spectrum β-lactamase-producing Klebsiella pneumoniae. The research emphasizes the role of hypervirulence-associated genes in this severe infection.

A rare case report details an oropharyngeal leech infestation in a child, leading to epistaxis and dysphagia. This case highlights the unusual presentations of leech infestations in pediatric patients.

A case report highlights myeloid sarcoma as an extramedullary blast crisis in a patient with BCR-ABL1 e6a2+ chronic myeloid leukemia (CML) complicated by myelofibrosis and tuberculosis. This finding may provide insights into the complex interactions between these conditions.

A case report highlights the TSHR Gly413Ser mutation's role in familial nonautoimmune hyperthyroidism. This discovery adds to the understanding of genetic factors influencing thyroid disorders.

A recent case-control study investigates the role of hepatocyte growth factor in children with primary ciliary dyskinesia, highlighting its potential relation to disease severity. This research contributes to understanding the biological mechanisms underlying this rare condition.

A new study highlights the diffuse sclerosing variant of papillary thyroid carcinoma as a rare and invasive cancer in childhood. This research underscores the challenges in diagnosing and treating this specific cancer variant.

A study published in PubMed reveals that early fibrotic remodeling in a rat model is responsive to autologous fat grafting. These histological findings could inform future therapeutic strategies for fibrosis-related conditions.

A recent study published in PubMed evaluates the efficacy of S-1 monotherapy for treating salivary duct carcinoma with MYC amplification. The findings contribute to understanding treatment options for this rare cancer type.

Not rare diseases news,
news about your rare disease.