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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.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Testosterone is crucial for development, growth, and various body functions in mammals.

Different hair loss types need accurate diagnosis for proper treatment.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

RNA can be extracted from horsehair roots for analysis.

Iron deficiency might contribute to hair loss in women.

Selenium can be toxic to animals, causing serious health issues, especially in horses.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

Mouse hair follicle stem cells lose their ability to change into different cell types after being grown for a long time.

Seasonal changes affect gene activity linked to hair growth in Angora goats, influencing mohair quality.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Mutation in hairless gene may increase hair loss risk.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.