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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Mimosine dipeptides are promising for treating hyperpigmentation and inflammation.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Cystic fibrosis can cause unusual symptoms like hair color changes, which can improve with proper treatment.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

A group has developed therapies that show promise for treating cancer and various other conditions.

PCOS and related metabolic issues often run in families.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

Manatee whiskers are specially adapted for touch in water.

The horse had a rare disease causing weight loss and skin issues, leading to euthanasia due to poor treatment options.

Musashi-2 limits epithelial cell movement and affects cell growth.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Mannan oligosaccharides improve raccoon dogs' fur quality and overall health.

Frontal fibrosing alopecia may run in families.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

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A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

CARASIL can cause different symptoms even with the same genetic mutation.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.