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About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Late-onset alopecia areata in Taiwanese patients is more common in women, usually starts at age 57, often involves less than 10% hair loss, and may have a minimal link to thyroid issues.

A gluten-free diet and surgery fixed the girl's calcium levels and started puberty.

Ovarian drilling surgery is not clearly better than medical treatments for PCOS symptoms.

A Moroccan athlete got a rare scalp infection, stressing the need for better hygiene in sports.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

A rare skin tumor with bone formation was successfully removed without recurrence.

An ovarian tumor can cause high male hormones in postmenopausal women.

Ovarian hyperthecosis caused high testosterone and virilization symptoms in a 60-year-old woman, which improved after surgery.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

The RAS pathway affects hair growth differently in CFCS and CS.

A baby with KID syndrome died from infections and organ failure at 18 months old.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Graves' disease can cause hair loss in children and should be considered when treating pediatric alopecia areata.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A postmenopausal woman's hirsutism and high testosterone levels improved after surgery for an ovarian tumor not seen on ultrasound.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Two babies needed surgery to remove hair tightly wrapped around their toes to prevent serious injury.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Scalp biopsies are important for diagnosing hair loss conditions.

OnabotulinumtoxinA treatment improved hair-pulling disorder and hair regrowth in a woman with chronic migraines.

A woman's high testosterone levels were caused by a rare ovarian tumor, not the initially diagnosed condition.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.