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The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Women with excess body hair feel psychological distress influenced by societal beauty standards, but distress isn't directly linked to the amount of hair.

Misdiagnosis led to permanent hair loss, stressing the need for proper scalp tests.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

A woman's hair loss was misdiagnosed as alopecia areata but was actually lichen planopilaris, needing immediate and ongoing treatment.

Stem cell treatment improved hair density in female hair loss patient.

A postmenopausal woman's excess male hormone symptoms were caused by a rare adrenal gland tissue in her ovary.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Some people with the skin color loss condition, vitiligo, also develop the skin inflammation condition, lichen planus, possibly due to local trauma, sun damage, or genetic factors.

A dog with unusual skin lesions near its tail was successfully treated for a rare form of lupus.

Early treatment with corticosteroids improved her eye condition significantly.

Finding a positive nonsentinel lymph node in melanoma patients indicates a worse prognosis.

The ShorT method can detect and help reduce bias in medical AI by identifying shortcut learning.

An 8-year-old boy's early puberty was caused by a rare hormone-secreting brain tumor, which was successfully treated with surgery.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

Infant baboons suffered from zinc poisoning due to poor cage conditions.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

Olanzapine helped a man who thought he had bugs on his skin.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

A 71-year-old woman developed male-like features due to high testosterone levels caused by a benign ovarian tumor, which was successfully removed by surgery.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.