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People with Lichen planopilaris are more likely to have certain autoimmune and endocrine disorders but less likely to have conditions like allergies and diabetes.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The treatment showed high response rates and was well-tolerated, potentially extending patient survival.

A young woman had a rare scalp tumor usually found in older women.

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

A new method accurately measures clobetasol propionate in hair and skin.

Cutaneous epitheliotropic lymphoma in dogs is often misdiagnosed but can be treated with chemotherapy and alternative therapies.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Thorough evaluations and conservative management can lead to positive outcomes in pediatric adrenocortical carcinoma.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Fatp4 is crucial for healthy skin development and function.

Higher levels of PD-L1 are linked to more severe hair loss in people with Alopecia Areata.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Calcium pantothenate therapy improved symptoms of discoid lupus erythematosus without side effects.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

Mycophenolate mofetil effectively improved skin pigmentation and itching in a woman with lichen planus pigmentosus and frontal fibrosing alopecia.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Lysophospholipids can act as anti-inflammatory agents through specific receptors, but more research is needed.