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Woman's hair loss diagnosis changed from CTE to AA; multiple biopsies important for accurate diagnosis.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

The document explains the genetic causes and characteristics of inherited hair disorders.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Red and infrared light therapy improves hair growth in balding patients.

Understanding skin structure and development helps diagnose and treat skin disorders.

Newer retinoid drugs are effective for skin conditions but have significant side effects.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Alopecia areata is a reversible, autoimmune-related hair loss that can have significant emotional impact and uncertain treatment effectiveness.

Chemotherapy can cause various skin reactions, with hair loss being the most common, and proper diagnosis and treatment of these reactions are important.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Mammals might fail to regenerate not because they lack the right cells, but because of how cells respond to their surroundings, and changing this environment could enhance regeneration.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Msx2 and Foxn1 are both crucial for hair growth and health.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Nearly half of children with primary immunodeficiency disorders showed skin problems, often as the first sign of their condition.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

The conclusion is that acne, alopecia, and hyperhidrosis are common skin issues with various treatments available, and accurate diagnosis is key for effective management.

Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.