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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The modified stem cells with VEGF165 in a special scaffold improved blood vessel growth and wound healing for skin repair.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

Certain growth factors can promote hair growth in mice by activating hair growth-related proteins.

The new delivery system could improve pain and inflammation relief in gout.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

IGF-1 increases whisker growth in transgenic mice.

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A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Combining plasma rich in growth factors with hair transplant surgery may lead to faster recovery and better outcomes for hair loss treatment.

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Mushroom-based scaffolds help heal skin wounds and regrow hair.

Folliculin slows hair growth, and blocking it might help treat hair loss.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

New punch designs for hair transplants have expanded options for surgeons.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

FUE is recommended as the initial choice for hair transplant on skin grafts.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.