Articles tagged with Skin Disorders
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Adults with a history of allergic disorders are at increased risk of developing high blood pressure and coronary heart disease. Asthma is the primary contributor to this risk, particularly among Black male adults.
Researchers found that seven patients with inflammatory skin conditions experienced anaphylaxis after using goat's milk or cheese products. The study highlights the potential risks of using foodstuffs as therapy for inflammatory skin conditions, leading to new allergies.
A recent report by the International Society of Microbiota confirms a bidirectional interplay between gut microbiota and various organs, highlighting the crucial role of microbiota in disease pathogenesis. The report also explores therapeutic strategies for manipulating gut microbiota to prevent and treat disorders.
Researchers found that elevated blood levels of two cardiovascular markers are associated with higher risks of cardiovascular problems in psoriatic disease patients. The study suggests a potential clinical tool for assessing heart health, but ordering tests is not recommended for asymptomatic patients.
A UC Davis Health study found that taking bile acids or treatments regulating their production levels can help control psoriasis inflammation. Bile acids inhibited skin inflammation by stopping immune T cells from producing proinflammatory protein IL-17A and blocking immune cell movement to the site.
A recent study published in Canine Medicine and Genetics found that French Bulldogs have a significantly higher risk of being diagnosed with 20 common health disorders compared to other breeds. The authors propose breeding towards more moderate characteristics to reduce these risks.
A new study suggests that Black children are more likely to be affected by a rare immune disease that causes scar tissue to form on skin and internal organs. The research found that one in five cases of the disease involve children under 16 years old, with over 90% of these being Black.
Researchers identified two distinct clusters of patients with Prurigo nodularis: those with increased inflammation and those with a higher likelihood of spinal disease. This study suggests that personalized treatment approaches can be tailored to specific patient profiles.
New study reveals that blocking interleukin-23 is more effective than targeting both interleukin-23 and interleukin-12 in treating psoriasis. Interleukin-12, previously thought to contribute to the disease, actually protects against it by maintaining normal skin cell function.
A four-year multicentre study by Ruhr-University Bochum's Department of Dermatosurgery found that adalimumab can be used both before and after surgery for moderate to severe hidradenitis suppurativa. The study involved 200 patients and showed the drug to be effective and safe in this context.
A recent study has identified specific miRNA signatures associated with EGFRI-induced skin rash, suggesting potential treatment-dependent biomarkers for this common side effect. The research found that miR-21 and miR-520e serum concentrations were negatively correlated with the severity of skin rash.
Researchers developed a classification algorithm that uses orchard data to predict internal browning, surface cavities and fruit firmness in apples with high accuracy. The method shows promise for improving yield and reducing losses in the fruit industry.
A whole foods, plant-based diet has been shown to ease the symptoms of livedoid vasculopathy, a blood vessel disorder causing painful ulcers on the feet and lower legs. The condition affects mostly women in their 30s, with poor blood flow being a contributing factor.
A study published in Scientific Reports reveals that mutations in a gene underlying a rare skin disorder can also lead to arrhythmogenic right ventricular cardiomyopathy, a serious heart disease. The findings indicate that the genetic underpinnings of skin disorders at birth may help predict future heart problems.
Researchers have developed a simple skin test that can accurately diagnose Parkinson's disease by detecting clumping of the protein alpha-synuclein. The assay was tested on 50 skin samples from patients with Parkinson's disease, achieving high sensitivity and specificity rates, promising an earlier diagnosis and better clinical trials.
A new hereditary disease, FACAS, has been discovered that causes a cold-induced urticarial rash in patients exposed to temperatures below 15°C. The researchers found that the disorder is caused by a previously unknown mutation in the 'Factor 12' gene.
Researchers developed an AI algorithm that can classify cutaneous skin disorders, predict malignancy, and suggest primary treatment options. The algorithm improved the diagnostic accuracy of clinicians, including dermatologists and the general public, by up to 86.8%.
A novel multisystem disorder has been identified due to bi-allelic variants in the CCDC47 gene, affecting individuals with symptoms such as woolly hair, liver dysfunction, and global developmental delay. The study demonstrates the importance of CCDC47 in normal development and highlights the need for further research into this condition.
Dr. Mandeep R. Mehra proposes a novel explanation for the Mona Lisa's smile and facial features, attributing them to clinical hypothyroidism. The theory is supported by visible signs of thyroid dysfunction in the painting, including thinning hair and yellow skin.
Researchers analyzed medical records of 487,104 black women and found that those with CCCA had a significantly higher prevalence of uterine fibroids compared to controls. The findings suggest a possible link between the two conditions, warranting increased awareness among physicians and patients.
A research team from Columbia University has developed a molecular taxonomy for hair disorders, which will help diagnose diseases affecting the hair follicles. The taxonomy was created by analyzing more than three million data points and identified nearly 5,000 biological terms shared by groups of hair genes.
Researchers discover misfolded prion proteins in skin samples from Creutzfeldt-Jakob disease patients, but find lower amounts in the skin compared to brain tissue. The study raises concerns about possible transmission of prion diseases through surgical procedures involving the skin.
Researchers developed a test to predict bitter pit disorder in stored Honeycrisp apples, which can save growers millions of dollars annually. The test analyzes calcium levels in fruit peels and indicates whether the disorder will develop.
Researchers linked lower levels of WNT10A protein to male pattern baldness and found a treatment mechanism involving beta-catenin signaling. Small molecule drugs targeting this pathway may treat hair thinning and palm skin defects in WNT10A patients.
A novel gene defect has been identified as the cause of a severe skin blistering disorder in Central Asian Shepherd dogs. The defect, found in the COL7A1 gene, leads to the absence of collagen, causing fragile skin and blisters.
Researchers identified a genetic mutation responsible for keratolytic winter erythema (KWE), a rare skin disorder prevalent among Afrikaners. The discovery enables dermatologists to diagnose KWE in patients and provides a starting point for developing potential treatments.
Patients with hyperpigmentation are more likely to use sunscreen, but few report reapplying it regularly. The study found that women and white/Hispanic patients were more likely to wear sunscreen, highlighting the importance of targeted education for these groups.
Research reveals that depression is linked to arthritis and digestive system diseases, while anxiety disorders are followed by skin diseases. A strong association was also found between epilepsy and eating disorders.
A new study found that patients with rare primary immunodeficiency disorders may be susceptible to serious side effects from the rubella vaccine. The study analyzed data from 14 patients and found that 7 had evidence of persistent rubella virus in their granulomas, leading to skin damage and ulcers.
Researchers at The Hebrew University of Jerusalem have developed a nanotechnology-based delivery system that activates the body's natural defense against free radicals. This system could control various skin pathologies and disorders by inducing antioxidant enzymes and maintaining skin cell redox balance.
Researchers from Loyola University Medical Center identified 60 genetic diseases that involve the skin, central nervous system, and/or peripheral nervous system. These conditions, including neurofibromatosis, can cause a range of symptoms such as tumors, learning disabilities, and bone deformities.
Researchers have discovered that two antioxidant supplements, N-acetylcysteine and glutathione, are effective in treating skin-picking disorder in mice. The study suggests that people with the condition may benefit from this therapy, which could potentially lead to fewer side effects compared to existing treatments.
A recent study reveals a significant association between hair disorders and susceptibility to dental caries. The research found that polymorphisms in hair keratins are associated with increased risk of dental defects and caries, highlighting the importance of keratin components in tooth enamel structure.
Researchers found that increasing fruit surface wetness increases severity of skin spot, a disorder characterized by patches of small brownish dots on apples' skin. The study also showed that skin spot is positively correlated with the number of rainy days during the growing season.
A new study finds that shingles significantly increases the risk of stroke in the first six months after symptoms appear. However, patients treated with oral antiviral medication for their shingles may experience lower stroke risks compared to those not treated.
The 'human hairless' gene plays a crucial role in regulating hair growth, with mutations contributing to atrichia with papular lesions. Researchers discovered the gene's histone demethylase function, offering hope for developing new approaches to treat skin disorders and rare forms of hair loss.
A new statistical risk model has been developed to assess arsenic contamination in China's groundwater. The model predicts that almost 20 million people live in high-risk areas with arsenic concentrations above 10 µg/L, highlighting the need for targeted sampling campaigns and increased monitoring efforts.
Scientists have identified a genetic mutation causing punctate palmoplantar keratoderma (PPPK), a rare skin disorder characterized by thick patches on hands and feet. The AAGAB gene mutation leads to hyperproliferation of skin cells, similar to common warts.
Researchers at Mount Sinai School of Medicine have found a potential treatment for craniosynostosis and acanthosis nigricans, two birth defects associated with Beare-Stevenson cutis gyrata syndrome. Inhibiting the protein p38 improved skull and skin defect outcomes in mouse models.
Two scientists, Elaine Fuchs and Howard Green, have been awarded the March of Dimes Prize in Developmental Biology for their groundbreaking research on skin stem cells and inherited skin disorders. Their work has saved thousands of lives and holds promise for new therapies for baldness and other diseases.
Researchers found a genetic link between Shar-Pei dogs' characteristic wrinkled skin and periodic fever disorder. The mutation is caused by an over-activation of the hyaluronan synthase 2 (HAS2) gene, leading to excessive hyaluronan production.
Patients who develop an acne-like skin rash after starting chemotherapy and cetuximab treatment have better overall survival, progression-free survival, and response rates compared to those without a rash. The study suggests that an early skin rash could be a predictor of treatment success in lung cancer patients.
A study of 90 patients with bullous pemphigoid found that nearly half had at least one neurologic disease, including cerebrovascular disease and dementia. The condition was often diagnosed after the neurologic disease, suggesting a potential predisposition.
A study by Johns Hopkins Medicine reveals that a rare inherited disorder called stiff skin syndrome shares genetic similarities with the debilitating condition scleroderma, affecting about one in 5,000 people. The findings suggest a potential treatment strategy involving the protein fibrillin-1 and its role in regulating TGFbeta activity.
Researchers at UT Southwestern Medical Center have identified distinct traits in patients with atypical progeroid syndrome (APS), a rare premature aging disorder. The study found that APS patients exhibit unique clinical features, metabolic abnormalities, and delayed onset of symptoms, potentially explaining their longer lifespan.
A new tool called Color Test (CT) was implemented in the Tomato Analyzer (TA) software to analyze color in fruits and vegetables. The study found that CT accurately captured and described characteristic colors for various crops, including tomatoes and strawberries with nonuniform pigmentation.
Researchers have found that bone marrow-derived stem cells can increase production of the col7 protein and form anchoring fibrils, improving the connection between the dermis and epidermis. This treatment has shown promise in increasing survival time and reducing blister formation in mouse models of the disease.
A collaborative effort by Boston University researchers has discovered the TFAP2A gene is linked to Branchio-Oculo-Facial syndrome (BOFS), a disorder marked by clefting, skin anomalies, and eye abnormalities. The study's findings may lead to more precise diagnostic testing and suggest new research directions.
Dr. Peter H. Byers has received the March of Dimes/Colonel Harland Sanders Award for Lifetime Achievement in Genetics for his groundbreaking research on collagen gene mutations and their role in inherited disorders such as Ehlers-Danlos syndrome and osteogenesis imperfecta. His work has significantly advanced our understanding of these...
A study published in Dermatologic Therapy reveals that rituximab effectively treats blistering skin diseases, including paraneoplastic pemphigus, by targeting abnormal immune responses. The drug's efficacy is being explored for other serious dermatological disorders, but its indications are still being defined.
Researchers have identified a natural compound, sulforaphane, found in broccoli that may treat a genetic skin disorder called epidermolysis bullosa simplex (EBS). Sulforaphane has been shown to induce the production of missing keratins in basal epidermis, potentially restoring skin integrity in EBS patients.
A study published by the American Academy of Neurology found that people with migraines have a thicker somatosensory cortex area, which processes pain and sensory information. This could lead to increased sensitivity to stimulation and contribute to other pain disorders.
Researchers at the University of Pennsylvania School of Medicine have found that adult mice can regenerate hair follicles by re-awakening dormant embryonic genes. This breakthrough could lead to new treatments for hair loss, scarring alopecia, and other skin disorders.
A new Stanford University School Medicine study finds that nearly as many men as women experience compulsive buying disorder, which is marked by binge buying and financial hardship. The study's findings contradict the widespread belief that most compulsive buyers are women.
Researchers at LIAI have identified Borrelia burgdorferi's glycolipid as an immune system trigger for fighting Lyme disease. This discovery could lead to the development of a new vaccine against the tick-borne disorder.
Researchers found a defect in the ATP2C1 gene causing type 2 mosaicism in Hailey-Hailey disease. Skin cells from patterned lesions possessed the mutant gene, while others had the normal chromosome.
A new study suggests that using stents to open blocked blood vessels in branching passages can lead to a harmful blood flow pattern, resulting in rapid re-occlusion of the main branch. This contradicts previous findings that suggest stenting was more successful in non-bifurcated areas.
Researchers have developed an antigen-specific ELISA test to diagnose lichen sclerosus by detecting circulating autoantibodies to extracellular matrix protein 1. This breakthrough diagnostic tool has the potential to improve disease management and treatment outcomes.
A recent study examined 350 adult volunteers and found that 3.6% developed harmless skin rashes after vaccination. The rashes cleared up on their own within one to three weeks without serious symptoms.
Researchers have identified a new tick-borne disease in North Carolina and the Southeast that is distinct from Lyme disease. The disease, caused by an unknown organism, produces symptoms similar to ehrlichiosis but without a telltale rash. Investigation led by Dr. Kathryn Kirkland suggests the infection can be cured with antibiotics.