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Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Minoxidil reacts to nitrosation 7 times more than phenol, mainly due to its -NH₂ groups, leading to the creation of N-nitrosominoxidil.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Elderly men with a scalp condition healed in about 26 days using specific creams and dressings, with no return of the condition in 6 months.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Hair transplantation and micrografting, used for baldness, involve moving hair follicles from hair-rich to bald areas, requiring careful procedure and post-care for success.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Using minoxidil and tretinoin on the skin, along with oral vitamin D, improved hair thickness and density in two girls with woolly hair.

Some treatments for autoimmune hair loss work, but JAK inhibitors like tofacitinib are promising for regrowth.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

Frontal Fibrosing Alopecia needs better diagnostics and treatments, with dutasteride showing promise.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Genetics, nutrition, lifestyle, and hormones affect early grey hair, but more research is needed.

A nurse-led hair service reduced waiting times and improved patient satisfaction and outcomes for alopecia areata treatment.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

PRP combined with Ayurvedic medicine may effectively treat hair loss.

The trichoscopy-assisted hair pull test is useful for diagnosing different types of hair loss.

BMP signaling is important for skin color, affecting melanin production, pigment spread, and cell movement.

Blocking a specific immune cell signal can trigger hair growth.

The research found that a specific skin cell type not only triggers hair growth but also controls hair color, and that aging can lead to hair loss and color changes.

Researchers found that the Leptin receptor is a consistent marker for hair follicle dermal cells, which may help future hair research.

Fgf20 is important for the development and regulation of the cells that form the base of hair follicles.