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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Oral tofacitinib significantly improves lichen planopilaris symptoms without adverse effects.

A rare scalp condition was successfully treated with specific medications after 9 months.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

SeV-Tp speeds up healing of drug-resistant infections by targeting wounds and killing bacteria with light activation.

Exosomes show promise as effective treatments for autoimmune skin diseases with fewer side effects.

Trichomycosis axillaris is a treatable bacterial infection of underarm hair.

Fibroblast-derived growth factors and exosomes can significantly improve skin aging.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

Survivors of Stevens-Johnson syndrome/toxic epidermal necrolysis need ongoing care for various long-term health problems.

Botulinum toxin injections effectively relieve pain from cutaneous leiomyomas.

Injecting specific cells into the skin can help improve skin structure and reduce blisters in a genetic skin disorder.

OnabotulinumtoxinA is used to treat wrinkles, pain, sweating, hair loss, and more by temporarily paralyzing muscles and affecting pain pathways.

Botulinum toxins show promise in treating various conditions, but more research is needed for hair and scalp disorders.

A man developed a skin reaction from metronidazole, which improved after stopping the drug and starting steroids.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Activating autophagy might reverse skin fibrosis.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

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.

Adipose tissue-derived exosomes may help treat lichen planopilaris and preserve hair.

Combining FTSC with TSN6 peptide greatly improves wound healing.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

A rare skin condition causes red and dark patches on the face and limbs.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A specific gene mutation causes a severe skin disorder in a family.