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A new DSG4 gene mutation causes hair defects in a young girl.

Sgk3 is essential for normal hair follicle growth and maintenance.

Acquired perforating dermatosis often affects skin in people with kidney issues and diabetes.

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

JAK inhibitors helped treat hair loss in two people with Down syndrome.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Diphenylcyclopropenone is more effective and has fewer side effects than dinitrochlorobenzene for treating alopecia areata.

Alopecia in VDR knockout mice is due to impaired hair cycle initiation, not keratinocyte issues.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Alopecia in VDR knockout mice is due to a defect in hair cycle initiation, not keratinocyte issues.

Deuterium oxide extends the hair cycle duration in mice without changing hair structure.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Skin side effects from CDK4/6 inhibitors in breast cancer patients are generally mild and treatable, allowing most patients to continue treatment.

UC.145 may be a new biomarker for predicting gastric cancer.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

DRDE-07 shows promise for treating skin diseases due to its favorable properties.

Akt2 and SGK3 are both important for normal hair growth and development.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

New mutations in the DSG4 gene cause a rare hair condition.

Mice without certain skin proteins had abnormal skin and hair development.

A new genetic mutation was found causing hair and eye issues in a boy.

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

JAK inhibitors may help treat alopecia areata by reversing hair loss.

Understanding genetics is crucial for treating heart and skin diseases.

Ornithine decarboxylase is crucial for hair growth regulation in mice.

A rare scalp tumor involving two hair follicles was successfully removed with surgery, with no recurrence after 7 months.