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A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

The hair coat disorder in Schipperkes is similar to Alopecia X and involves increased androstenedione levels and hair cycle arrest.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

A gene mutation in mice causes skin defects and early death.

Neonate scalp hair is thinner, lacks a medulla, and has smaller follicles compared to adult hair.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.