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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Metformin and liraglutide improved symptoms of HAIR-AN syndrome in a child.

New genetic mutations causing hair loss were found in a Chinese family.

Chronic lupus and frontal fibrosing alopecia can occur together, but their connection is unclear.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.

PFS might be a delusional disorder with potential to become mass psychogenic illness.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Hair transplant destroyed by lichen planopilaris.

EFFC might be common but underreported.

Many Korean women with female-pattern hair loss have reduced hair density at the temples.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The free androgen index varies among women with different types of PCOS.

Contact allergies might contribute to frontal fibrosing alopecia.

FAI is a better marker for predicting female hair loss than testosterone or SHBG alone.

Using superficial temporal fascia helps prevent Frey syndrome after parotid surgery.

The same gene mutation can cause different symptoms in family members.

The document concludes that there are no reliable treatments for frontal fibrosing alopecia, with only temporary benefits from current options.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A 66-year-old man with a rare case of male frontal fibrosing alopecia did not regrow hair despite treatment.

Hair loss improved after removing pituitary tumor.

The Fas/FasL pathway may play a role in alopecia areata.