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Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Antiandrogen therapy helped increase hair growth in women with hormonal imbalances related to baldness.

Mutations in the KRT85 gene cause hair and nail problems.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

A patient had skin tissue death at the hair removal site after a hair transplant, which was treated with surgery.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Increasing Wnt5a in mice skin delays hair growth but doesn't stop it.

Researchers found a new mutation causing total hair loss from birth.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

Hair and wool have diverse keratins and keratin-associated proteins.

Polycystic ovary syndrome is the main cause of hirsutism in premenopausal Iranian women.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Many women with hair loss also have thyroid issues, high blood pressure, and low Vitamin D.

The cause of alopecia areata was unknown, and while various treatments existed, no best treatment was agreed upon.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Diphencyprone can cause unexpected and possibly permanent vitiligo.

Finasteride caused blisters on hands and feet.

A woman developed vitiligo from repeated eyebrow microblading.

White and yellow dots indicate severe female hair loss in dark skin.

Denosumab treatment for osteoporosis can cause hair loss.