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

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

The girl has a genetic hair condition causing thin hair since childhood.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair loss patterns differ between males and females due to 5 master regulators and JAK-STAT signaling affects hair growth.

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

No link found between specific genes and female pattern hair loss.

Early diagnosis and personalized treatments are crucial for better hair loss management.

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

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Genetic factors affecting skin health and body weight may increase the risk of dermatophytosis.

Genetic marker rs12558842 strongly linked to male hair loss.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document concluded that FDA-approved treatments like minoxidil and finasteride are effective for hair loss, while the effectiveness of natural remedies and other non-approved treatments is not well-supported by evidence.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.