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A new, efficient method has been developed to detect darolutamide and thalidomide, drugs used for certain hair loss and prostate cancer treatments, in pharmaceuticals and body fluids.

Madarosis (eyebrow and eyelash loss) significantly affects quality of life for breast cancer patients on taxane-based chemotherapy.

Adenosine helps grow thicker hair in Japanese men with hair loss.

Acne is common in adult women, often continues from adolescence, and can lead to scarring.

SIG-1451 could be a promising new treatment for atopic dermatitis.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Algerian Carthamus caeruleus L plant has anti-inflammatory properties, heals wounds effectively, and may help with hair growth.

Diabetes rates in Saudi Arabia are rising, especially Type 2, with more men affected, and will continue to increase by 2030.

Early diagnosis and treatment of hair loss in hijab-wearing women are crucial to prevent permanent damage and improve quality of life.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Clinicians should look for skin issues, sleep problems, cognitive changes, and food cravings as signs of insulin resistance.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

Premature greying of hair is common among young people at King Faisal University, especially females, and is linked to health issues, lifestyle, and family history.

High doses of dihydroartemisinin caused reversible liver toxicity in rats, with females more affected than males.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Astragaloside A may help fight lung cancer by targeting specific proteins.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

A specific gene mutation causes sparse, brittle hair in a family.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Combining dutasteride mesotherapy with oral minoxidil is more effective for hair loss than using oral minoxidil alone.