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

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

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.

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

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

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.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair loss linked to higher heart disease risk in both men and women.

Skin tags in obese individuals may indicate higher cardiovascular risk.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

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

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.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

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

LLLT helps treat hair loss by increasing blood flow, reducing inflammation, and stimulating growth factors.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

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

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Certain growth factors significantly affect hair loss in women with telogen effluvium.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

People with early-onset hair loss (AGA) have a higher risk of heart disease, metabolic syndrome, and prostate enlargement.