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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

A young boy with Netherton syndrome improved significantly using IVIG, dupilumab, and dietary changes.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Long scalp hair evolved for cooling and social signaling.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Some hair protein genes evolved early and were adapted for use in hair follicles.

Zebrafish skin regeneration relies on cell behaviors and reactive oxygen species, with antioxidants reducing and hydrogen peroxide increasing regeneration.

VDR regulation varies by tissue and is crucial for its biological functions.

Witch hazel is effective for skin care due to its antimicrobial, anti-inflammatory, antioxidant, and healing properties.

Melanocytes in different body areas have evolved to perform specific functions based on their location.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

New small molecule drugs show promise in treating complex skin diseases but need more safety research.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

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

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

No link found between new male baldness genes and female hair loss.

No link found between specific genes and female pattern hair loss.

Hairless gene not strongly linked to baldness.

Six new hair loss factors in men not linked to female hair loss.

MC4R gene variants not linked to female hair loss.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Biotin supplements significantly improved a young girl's uncombable hair.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.