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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Enzymes called PADIs play a key role in hair growth and loss.

A patient with Ehlers-Danlos Syndrome improved after treatment for fat malabsorption and essential fatty acid deficiency.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

Activating ALDH2 can boost hair growth.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

UC-MSC-derived exosomes may help treat hair loss by promoting hair cell growth through AKT activation.

Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Hair diameter diversity could improve androgenetic alopecia assessment and treatment planning.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

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

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

Squaric acid dibutylester effectively treats alopecia areata.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

MCHR2 gene duplications may be linked to alopecia areata.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Men with male pattern baldness have higher levels of A-FABP, which might help in early detection.

Men taking dutasteride may have a higher risk of age-related macular degeneration.

The humanized AA mouse model is better for testing new alopecia areata treatments.

A new mutation in the HR gene causes hair loss in a specific family.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

ADAM 10 and ADAM 12 proteins are involved in different stages of hair growth and could be targets for treating hair disorders.