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Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

AGA risk factors include age, smoking, hypertension for men, and age, dyslipidemia for women; lifestyle changes may help prevention.

DDAIP-HCl significantly increases minoxidil absorption into the skin.

The BASP classification is a detailed and accurate way to categorize hair loss in both men and women.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Long-COVID has diverse, long-term health impacts, especially in young people.

Nails can reveal important health information about skin and body conditions.

Vimentin and transthyretin proteins are linked to black coat color in sheep.

The document concludes that while some hair and scalp disorders can be treated, hair loss from destroyed follicles is permanent, and damaged hair can only regrow naturally.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

PCOD mainly affects young women, causing symptoms like irregular periods and weight gain, with mixed success from lifestyle changes and medication.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Certain Ayurvedic herbs may help manage premature greying of hair.

Hoxc13 is linked to seasonal hair growth in Cashmere goats and is affected by melatonin.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

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

Minoxidil applied twice daily can help regrow hair in some people with hereditary baldness, with no serious side effects.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A girl had rickets due to a gene mutation affecting vitamin D response.

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

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

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

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

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

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

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.