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A genetic marker linked to a type of hair loss was found in most patients studied.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

High PMP 22 levels in type 2 diabetes patients may cause hearing loss.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

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

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mdm2 is crucial for controlling p53 to maintain healthy cells and prevent tumors.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

TSLP affects atopic dermatitis by increasing sebum and reducing fat through IL-4/IL-13 signaling.

The document concludes that more local research on African skin and hair is needed despite increased scientific output from Sub-Saharan Africa.

A gene mutation in Lama3 is linked to a common type of hair loss.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

SCD1 is crucial for skin health and overall energy balance.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

New genetic discoveries may lead to better treatments for alopecia areata.

Melatonin, a hormone, can help protect skin from aging by reducing stress, inflammation, and damage, and may also help treat hair loss in women.

The Gsdma3 gene is essential for normal hair development in mice.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Thyroid and skin autoimmune diseases share genetic and immune links, affecting both tissues.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Targeting JAK-STAT1 can reduce inflammation and promote hair growth in conditions linked to EGFR deficiency.

Iron deficiency in menstruating women causes many health issues beyond anemia and needs early detection and treatment.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.