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CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Early balding linked to higher heart disease risk.

Glucocorticoid treatment improved symptoms in a girl with Satoyoshi disease.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Widened sweat ducts are a very specific sign of scarring hair loss.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

Demographic factors like age, education, and marriage duration affect mindfulness in women with PCOS.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Artemis dysfunction might cause hair loss through telomere shortening.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

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The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A woman developed a hair disorder after a bone marrow transplant, which improved with treatment.

Fibrosing alopecia in a pattern distribution is a type of hair loss that may often be overlooked, especially in men.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

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

Individuals with this condition often develop male traits and identities at puberty despite being raised as females.

Androgenetic alopecia may cause schizophrenia, but schizophrenia does not cause androgenetic alopecia.

Cantú syndrome may be linked to pituitary adenomas.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

Dermoscopy is useful for early diagnosis and monitoring of nail diseases.

A gene mutation in mice causes severe skin disorder similar to a human condition.