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The combination of stem cell medium and hydrogel effectively reduces and improves hypertrophic scars.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

Insurers opposed ASCO's recommendation for a single cancer care pathway program.

PCOS care in Singapore can be bettered by refining referral systems, standardizing diagnosis and treatment, enhancing complication screening, and offering educational resources for clinicians.

A woman with severe hair loss due to systemic sclerosis regrew her hair in 4 months using a combination of treatments.

New treatments for chronic central serous chorioretinopathy show promise in preventing permanent vision loss.

The method shows how hair lipids form specific patterns and their roles in hair structure.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

New standards were created to make chemotherapy safer and improve cancer care.

A young man was unexpectedly diagnosed with basal cell carcinoma after a scalp examination and confocal microscopy.

Reflectance confocal microscopy can help tell apart scarring from non-scarring hair loss.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The new classification system for skin disorders emphasizes the importance of understanding a patient's awareness of their condition for better treatment.

ADSC-CE treatment safely increases hair density and thickness in androgenetic alopecia patients.

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

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

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

PTCH gene mutations contribute to basal cell carcinoma development.

The research suggests new treatments for skin cancer could target specific cell growth pathways.

Mohs micrographic surgery is effective for treating basal cell carcinoma on the eyelid, while radiotherapy has higher recurrence rates, and topical vitamin D3 may reduce and delay BCC formation in mice.

The Scalp Coverage Scoring method reliably measures hair density from images.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.