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A 66-year-old woman experienced hair loss due to Frontal Fibrosing Alopecia, a condition with no consistently effective treatment, but it usually stabilizes over time. More research is needed for better understanding and treatment options.

The PCOSQ-50 is a valid and reliable questionnaire for measuring quality of life in Iranian women with PCOS.

Reflectance confocal microscopy is useful for diagnosing scalp melanomas, which have features similar to those on the trunk.

Longer CAG repeats in gene linked to more severe hair loss in females.

Cirsium japonicum flower extract increases melanin production and could help treat depigmentation conditions.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Combination therapy with steroids and pimecrolimus improved or stabilized hair loss in most patients with Frontal Fibrosing Alopecia, who also had a high rate of hypothyroidism.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Nelfb is essential for dermal fat development and survival.

A subtle androgen receptor abnormality can allow normal male development and sometimes fertility despite partial androgen resistance.

Ch55 may help reduce skin scarring and fibrosis.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A pet ferret had a serious infection from Mycobacterium xenopi, which can spread to humans.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

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Pair housing reduces stress behaviors and health issues in quarantined rhesus macaques.

SFRP-4 might be an early indicator of diabetes and hypertension in men with androgenic alopecia.

Most patients with frontal fibrosing alopecia are postmenopausal women, and treatments like finasteride and dutasteride can improve or stabilize the condition.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The new method provides more accurate vibrational frequencies for drug molecules than traditional models.

Testosterone boosts fluid and electrolyte secretion in seminal vesicles, aiding sperm function.