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The conclusion is that fat tissue in the skin is a new finding in Frontal fibrosing alopecia and may contribute to hair follicle and muscle degeneration.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

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

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

Testosterone Replacement Therapy can improve sexual health in postmenopausal women with low sexual desire, but more research is needed on its long-term effects.

The study found that baicalin has different stable shapes in gas and water, with two shapes better for interacting with positive charges in water.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

The document concludes that choosing the right face rejuvenation technique depends on the individual's unique features and aesthetic goals.

New microneedles deliver drugs through the skin accurately and effectively.

Pharmacy workers need more education to better help people with hair loss.

A single robotic system can accurately harvest and implant hair grafts, showing promise for real-world use.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Some dermatologists in Saudi Arabia prescribe Tofacitinib for hair loss, but many don't due to its unavailability and safety concerns.

EGFR is crucial for preventing hair follicle inflammation and hair loss.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The article suggests that hair transplant surgery may not be purely cosmetic because it treats a disease and calls for clearer guidelines on its classification.

The document provides a step-by-step training guide for beginner surgeons and assistants to learn hair restoration surgery, emphasizing careful practice to avoid irreversible loss of hair follicles.

Garg and Garg created an affordable, easy-to-use training program for hair restoration surgery using everyday items, which can teach a technician the basics in 3-4 weeks with two hours of daily practice.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The document concludes that choosing the right forehead and brow lifting technique based on individual patient characteristics is crucial to prevent complications and achieve desired results.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Hair transplant surgery should only be done by licensed professionals, as many states don't allow unlicensed personnel to perform it.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Babies born after 38 weeks to mothers under 36 years old and not delivered by C-section have a higher risk of neonatal occipital alopecia.

Different hair growth phases affect how follicles respond to X-rays, and hormones like testosterone and dihydrotestosterone play a key role in baldness; transplanted hair can grow on bald scalp areas.

Compound 7b is a promising candidate for treating benign prostatic hyperplasia and prostate cancer.

FUE hair transplant is effective and safe for treating hair loss.