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

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Ingesting Leucaena leucocephala caused hair loss and increased infant mortality in ringtailed lemurs.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

A woman on immunosuppressants developed two rare scalp conditions, which improved with specific treatments.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

People with lichen planopilaris often have seborrheic dermatitis, which can delay the diagnosis of lichen planopilaris.

A man had both alopecia areata and lichen planus, which is uncommon.

Hair loss in Lichen Planopilaris is caused by immune system issues damaging hair follicles and stem cells.

Monilethrix causes different levels of hair loss in family members.

A rare case showed alopecia areata and lichen planus occurring together in one person.

Vitamin B12 deficiency can cause reversible skin darkening.

Diode laser effectively treats pseudofolliculitis barbae.

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

The study found increased skin pigmentation and variable melanocyte density in a patient with Addison's disease.

Nilotinib can cause generalized keratosis pilaris.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Treat active lichen planopilaris early to prevent permanent hair loss.

Leprosy and psoriasis were historically confused, but were finally distinguished as separate diseases in the 1800s.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Intense Pulse Light effectively reduces hair growth in faun tail nevus.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.