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Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

Hair transplants can be a treatment for scarring hair loss if there's good blood flow and no active disease.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Doctors should diagnose hair loss by examining the patient and possibly doing tests, and then treat it based on the type, which may prevent permanent hair loss.

Hair follicles are important for drug delivery through the skin, but better methods are needed to understand and improve this process.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

Hair loss was found in 37.4% of surveyed rural high-school students in Eskisehir, Turkey, affecting their quality of life, especially in general health and mental well-being.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Alopecia areata in infants may be more common than previously thought.

Monilethrix causes different levels of hair loss in family members.

Androgenetic alopecia causes hair thinning due to increased androgen activity, treatable with minoxidil and finasteride.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.