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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

The ProScope HR is an effective, user-friendly, and affordable tool for diagnosing hair loss.

A unique gene mutation was found in a family with monilethrix.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

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

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Researchers developed a method to create artificial hair follicles that may help with hair loss treatment and research.

Patients with hair loss are much more likely to have body dysmorphic disorder than general dermatology patients.

The Swedish Hairdex-S is a reliable tool for assessing quality of life in Alopecia Areata patients.

THBS4 helps hair grow by activating hair follicle stem cells.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

3D ultrasound can detect hair follicle changes and disease phases in alopecia areata.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

Mutations in the DSG4 gene cause specific hair and scalp issues.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

DPP4, a molecule in skin, helps heal large wounds and regrow hair follicles when its levels are reduced.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

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

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Masculinization in affected individuals occurs gradually after puberty due to hormone changes.

DTDG in hair treatments reduces damage and preserves hair structure.

ApoBDs, once seen as waste, are now viewed as potential tools for disease treatment and tissue repair.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Myoblast transplantation shows promise for treating various muscle and heart conditions.