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Most types of hair loss can regrow naturally, but there are no effective cures for male pattern or age-related hair loss, and only limited options for females.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

VDR regulation varies by tissue and is crucial for its biological functions.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Using minoxidil on the scalp can help grow hair for people with hereditary baldness.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Some treatments for hereditary hair loss are effective but vary in results and side effects; new therapies show promise but need more research.

Caffeine may help hair growth in hereditary hair loss.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Finasteride treatment slows down hair loss, boosts hair growth, and may increase hair thickness or length, but it can cause side effects like decreased libido and depression in less than 1% of people.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

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

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Topical minoxidil showed promise for early male pattern baldness.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

ViviScal®, a food supplement, was found to be highly effective in treating hereditary hair loss in young males, while fish extract showed no impact.