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The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

The document explains different hair and scalp conditions, including common hair loss after pregnancy or illness, drug-induced hair loss, hereditary excessive hair growth, patterned baldness, autoimmune hair loss, and permanent loss due to skin disease, with generally limited treatment options.

Hair loss can be treated based on its type and cause, improving quality of life.

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

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Removing hair from mice without reproductive glands led to grey hair, possibly helping to understand greying in aging.

New hair loss treatments could be improved by using combined biological markers.

The girl's hair loss is due to trichotillomania, which may improve with behavioral therapy or a combination of treatments.

Lack of certain nutrients may contribute to hair loss and proper diet or supplements could improve it.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Scientists created a new 3D skin model from cells of plucked hairs that works like real skin and is easier to get.

Most men seeking hair transplants have Male Pattern Baldness, influenced by genetics, age, and testosterone, while women's hair loss can be affected by thyroid function, iron, testosterone, prolactin, ferritin levels, and certain conditions. Follicular Unit Extraction is a popular hair transplant technique.

Psychological factors significantly affect hair health, suggesting a need for integrating mental health care in treating hair loss.

New cells join the hair's dermal papilla during the growth phase, possibly affecting hair thickness.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Hair graying is caused by the loss of pigment cells due to poor maintenance of stem cells in the hair follicle.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

Hair loss can be treated with medications like finasteride and surgical methods like hair transplants.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

Hair loss caused by genetics and hormones; more research needed for treatments.

Two treatments for male pattern hair loss are minoxidil and finasteride, but they have side effects and may not satisfy everyone.

Hair loss is linked to eating less soy, having lower blood vanadium, and a specific genetic variation in Taiwanese communities.

The research found that certain genes are linked to male pattern baldness, but these same genes do not affect female pattern hair loss.

Fat-related cells are important for initiating hair growth.

Skin needs dermal β-catenin activity for hair growth and skin cell multiplication.

Lactate production is important for activating hair growth stem cells.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.