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Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The study suggests silicon might be important for healthy hair, as less silicon was found in people with hair loss.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Scientists improved how to make skin-like structures from stem cells using special gels and a device that controls growth signals, leading to better hair and skin features.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.