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A new method uses expert reviews of home videos to objectively assess children's developmental milestones in single-arm trials.

Dupilumab effectively treats severe skin issues in a rare genetic disorder.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Eyebrow and eyelash hair loss in alopecia areata worsens quality of life.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

A 2-year-old boy with a rare type of lupus causing hair loss improved with oral steroids.

Lambs fed a liquid diet showed abnormal wool and skin, which improved with more B-vitamins, suggesting a link to B-vitamin deficiency.

The endobrow-midface lift is a safe and effective way to rejuvenate the upper face with minimal complications and rare temporary hair loss.

A new type of mite caused hair loss in a koala, which was treated successfully with ivermectin.

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.

Two siblings both had a rare case of alopecia areata at the same time.

Melanocytes can regenerate around hair follicles in bullous pemphigoid, especially in patients with darker skin.

Choose the best brow lift method based on patient needs and goals.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Alopecia areata in infants may be more common than previously thought.

Permanent eyebrow correction can improve quality of life for those with eyebrow loss.

Azathioprine can help with relapses and disability in NMOSD but has more side effects and needs more research.

Eyelash restoration needs skilled experts for safe, natural results.

The simplified eyebrow transplant technique is safe, effective, and looks natural.

Adults can develop late-onset loose anagen syndrome, which may often be misdiagnosed.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

New tools help assess eyebrow, eyelash, and nail changes in Alopecia Areata, improving understanding of patient experiences.

Ultraviolet techniques help identify Grover’s Disease, which may be underdiagnosed in young people and females.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.