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Up to half of adult women may experience hair loss, and doctors should use medical history, exams, and tests to find the cause and treat it.

Biotin deficiency is not a major cause of hair loss in women, so biotin supplements are not likely to be an effective hair loss treatment.

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

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

The document concludes that each reviewed medical book is useful for its specific area in pediatric care, especially the "Neonatal Formulary" for neonatal drug information.

Severe acne in a young girl may indicate underlying hormonal issues.

Hair loss significantly lowers life quality, especially in young men, with most patients unhappy with treatment effectiveness.

Mutations in the AR gene cause hair thinning and loss.

Minoxidil and finasteride are key treatments for hair loss.

Certain Ayurvedic herbs may help manage premature greying of hair.

Ayurveda can prevent hair fall and promote regrowth using herbs and lifestyle changes.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

Glycerol may improve wound healing and prevent keloids, a device can measure itch intensity, male pattern baldness is highly heritable, and fumaric acid esters may work for psoriasis by causing cell death in T cells.

The products significantly promote hair growth and maintain hair bulb health.

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

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

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.

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

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

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.