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ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Haloperidol decanoate can cause alopecia areata.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Dermatoscopy can help identify hydroquinone-induced skin issues, avoiding invasive biopsies.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

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

The IBHRS is now operational.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Hairless protein can block vitamin D activation in skin cells.

Hair follicle cells help maintain and support stem cells and blood cell formation.

Increased 11β-HSD1 activity in skin may contribute to aging and could be targeted to reduce aging effects.

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Vitamin D receptor and hairless protein are essential for hair growth.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Trichoscopy is useful for diagnosing and monitoring hair and scalp conditions over time.

Hair follicle stem cells could lead to new hair loss treatments.

HLA can be linked to autoimmune hepatitis.

Several doctors received research grants, new workshops and conferences were announced, and new officers were elected.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

OCT can effectively examine and reveal details about human hair and scalp conditions.

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.