Search

everythinglearnresearchcommunity

for

Search:↓

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

Advancements in cosmetic and reconstructive surgery improve techniques and patient satisfaction.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

Vitamin A toxicity can cause severe health issues and may require a liver transplant if other treatments fail.

The study concluded that severity of Frontal fibrosing alopecia is not linked to how long someone has it, can start before menopause, and eyebrow loss may be an early sign.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

The document says doctors should identify and treat Frontal fibrosing alopecia medically before considering surgery, as treatments often don't work well.

The woman was diagnosed with lichen planopilaris and can be treated with corticosteroids.

The document concludes that there are no reliable treatments for frontal fibrosing alopecia, with only temporary benefits from current options.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

More pediatric-specific research and guidelines are needed to improve hidradenitis suppurativa treatment in children and adolescents.

Treatments for Frontal Fibrosing Alopecia have not been proven effective.

New genes and pathways are important for testosterone production and male sexual development.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

Stopping steroids and providing supportive care improved the patient's Cushing Syndrome symptoms and ulcers.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Hair removal with intense pulsed light can cause rare skin lesions that are hard to fully treat.

Trichoscopy can reliably distinguish between alopecia areata and trichotillomania.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A woman lost her hair from stress after a bee attack and her sister's death.

Hair loss in systemic lupus erythematosus patients is unique and improves with treatment.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Syphilis can cause hair loss and should be considered in unexplained cases.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.