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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Understanding how acne develops in different diseases could lead to new treatments.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

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

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Genetic predictions of baldness in Europeans don't apply well to African men.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Personalized treatments for hair loss are becoming more effective by using genetic information.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

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

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Removing a key gene in mice leads to premature aging and loss of stem cells.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

Human nails and hair follicles have similar gene activity, especially in the cells that contribute to their growth and development.

Keratin from human hair helps nerves heal faster.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Loose anagen hair syndrome may be caused by keratin gene mutations.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A rare gene variant causes hair and nail issues in a family.

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.

Imbalanced skin bacteria worsen diabetic foot ulcers, but adjusting them might improve healing.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.