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The arrector pili muscle might play a role in hair loss and needs more research to understand its impact.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Miniaturized hairs stay connected to muscle in alopecia areata, allowing possible regrowth, but not in androgenetic alopecia.

The document suggests simplifying alopecia diagnosis and improving techniques for better accuracy.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

AGA causes hair loss through follicle miniaturization and hair cycle changes; regrowth depends on anagen initiation in kenogen follicles.

Scalp hair grows at 0.37 mm/day, forearm hair at 0.18 mm/day, and thigh hair at 0.30 mm/day, with no significant differences found in people with certain hair conditions.

Only skin melanocytes, not other types, can color hair in mice.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Frontal Fibrosing Alopecia is a type of hair loss affecting mostly older women, with no agreed best treatment.

Hair loss in African American women, caused by hair care, genetics, and environment, needs more research for better treatment.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

Effective hair loss assessment requires a mix of precise measurement methods.

Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

Human hair follicle dermal cells can effectively replace other cells in engineered skin.

AcSDKP may help prevent skin and hair aging and promote their growth.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Chemotherapy and radiotherapy can cause skin side effects like rashes, hair loss, and nail changes, which are usually managed with conservative treatments.

Photodynamic therapy can remove nonpigmented hair in mice and might work for humans.

Different ectodermal organs like hair and feathers regenerate differently, with specific stem cells and signals involved in their growth and response to the environment.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

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

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Platelet-rich plasma (PRP) is a simple, cost-effective treatment that promotes hair growth and reduces hair loss, with high patient satisfaction.

Scaffold-based strategies show promise for regenerating hair follicles and teeth but need more research for clinical use.

Mutations in the LSS gene cause a rare type of hereditary hair loss.