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Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Nilotinib can cause keratosis pilaris, a skin condition.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Mitochondrial dysfunction and oxidative stress may play a role in Lichen Planopilaris.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Keratin gene clusters in humans and marsupials are similarly organized.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Platelet-rich plasma (PRP) is an effective treatment for lichen planopilaris.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Metabolic issues may trigger lymphocytic cicatricial alopecia, and treatments targeting these issues could help.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Mutant keratins cause inflammation in Epidermolysis Bullosa Simplex, suggesting targeting them could help treat the disorder.

Lichen planus pigmentosus and fibrosing frontal alopecia in Colombia are likely different stages of the same disease.

A young Caucasian man experienced a rare type of hair loss on the back of his head.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

Nilotinib can cause skin issues like red bumps and hair loss.

A 20-year-old had hair loss and skin issues from lichen planopilaris starting at age 10.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

Combining hair transplantation with PRP is more effective for treating hair loss than hair transplantation alone.

PPAR-γ agonists like pioglitazone may help manage lichen planopilaris but don't fully reverse scarring.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The study concluded that people with Lichen Planopilaris have a more diverse scalp bacteria and different metabolic pathways compared to healthy individuals.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Platelet-rich plasma therapy improves oral lichen planus symptoms with few side effects.

A dog with a hereditary skin condition causing blisters and hair loss survived for a year.

A new variant of lichen planopilaris causing diffuse hair thinning was identified.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

PP2Acα is essential for proper hair and skin development.