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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

Androgenetic alopecia in women needs more research and better management strategies.

The mini-lift is a less invasive face-lift for younger patients that is quicker, cheaper, and has a fast recovery, but is less effective for the midface and excessive neck skin.

Women who had cancer treatment feel both positive and negative about their bodies.

COVID-19 can cause hair loss starting as early as 18 days after infection.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Finasteride may negatively affect male fertility.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Loss of keratin K2 causes skin problems and inflammation.

XEDAR triggers a specific signaling pathway in cells.

LAAM caused developmental toxicity in tolerant rats without causing birth defects.

Alternating treatment with two drugs could help cells in a rapid aging disease.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.