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Autologous cell-based therapy using dermal sheath cup cells may help treat pattern hair loss, especially in women.

A 9-year-old girl with a healthy immune system was successfully treated for a severe fungal scalp infection caused by Microsporum audouinii.

About half the patients treated with capecitabine and docetaxel developed severe hand-foot syndrome.

SVF injections improve hair growth and reduce hair loss in people with androgenic alopecia.

One child resisted treatment, while the other was successfully treated for scalp ringworm.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

The new method isolates more hair follicle stem cells from mice quickly and these cells help promote hair growth.

Standardized kits improve the quality and consistency of isolating stem cells from fat tissue.

Long-hair follicular unit excision improves hairline restoration results and patient satisfaction.

A new tool simplifies alopecia areata severity scoring but needs validation.

3D spheroid culture makes stem cells better at reducing inflammation.

Early diagnosis and treatment are crucial for complex medical conditions.

Tangent screens help detect visual field defects from vigabatrin.

Platelet-rich Plasma Gel may help treat en coup de sabre scleroderma, improving symptoms and skin quality with minimal side effects.

The document provides a method to prepare human scalp tissue for studying hair follicles at the single-cell level.

Targeting the protein Caveolin-1 might help treat a type of scarring hair loss called Frontal Fibrosing Alopecia.

The platform effectively grows lung cancer cell spheroids for drug testing.

CCCA involves immune response and metabolism issues, suggesting new treatment options.

Potential therapeutic targets for scarring hair loss are identified.

MSC-EVs and UCB-EVs improve skin wound healing and reduce scarring.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A Japanese bone marrow transplant patient developed a rare skin cancer possibly linked to long-term use of the medication voriconazole.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

Melanocyte stem cells can become melanoma, resembling human melanoma.