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Puerto Rican children with cancer often experience symptoms like irritability, nausea, and hair loss, and need better education and continuous symptom management.

Early diagnosis and treatment of PCOS in young people is important to prevent long-term health problems.

A cancer drug caused unusual hair growth on a 100-year-old man's scalp and eyelashes.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Fractional laser treatment helped hair regrowth in patients with alopecia areata.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

Some children with localized scleroderma are rarely resistant to methotrexate, and no common profile for resistance was found.

Bariatric surgery is safe and effective for treating adolescent obesity.

Androgens can both increase body hair and cause scalp hair loss.

AGA in children needs careful diagnosis due to low androgen levels and possible other causes.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

T-cell reconstitution after thymus transplantation can cause hair whitening and loss.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Finasteride blocks deoxycorticosterone's anticonvulsant effects in infant rats, but indomethacin doesn't.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Male pattern baldness might have evolved to help protect against prostate cancer by increasing UV radiation on the scalp.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

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