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Professor Ma Shuanquan treats hair loss by using Chinese medicine to improve liver, spleen, and kidney health.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Lack of cystatin M/E causes thin hair and dry skin.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

In 2002, various skin reactions were reported due to different drugs, including allergies, hair loss, skin lesions, and other skin conditions.

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.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

Intralesional triamcinolone acetonide is more effective than platelet-rich plasma for treating scalp alopecia areata.

Diphenylcyclopropenone is more effective and has fewer side effects than dinitrochlorobenzene for treating alopecia areata.

Topical immunotherapy, especially with DPCP, is effective for treating severe alopecia areata.

AGA can occur in children with family history; early diagnosis and treatment important.

Intralesional corticosteroids are the best for limited alopecia areata, oral steroids are less effective, and PRP is safe and promising, especially for children and severe cases.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Type XVII collagen helps control skin cell growth and could be a target for anti-aging treatments.

Monilethrix is a rare genetic hair disorder that's hard to treat.

The document explains different types of skin lesions and their characteristics, causes, and related conditions.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

Gene mutations can cause problems in male genital development.

Androgenetic Alopecia (AGA) greatly lowers quality of life, causing stress and low self-esteem, with those seeking treatment experiencing more impairment.

Both DPCP alone and with PRP are effective and safe for treating severe alopecia areata.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Different ethnic groups have unique hair growth patterns, with African hair growing slower and less dense, Asian hair growing fast but sparse, and Caucasian hair being densest; men are more likely to experience hair loss than women.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.