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Non-scarring hair loss is common in lupus patients and can be diagnosed with specific hair and tissue tests.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

A teenager had both alopecia areata and vitiligo, which are rare to occur together.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

Forensic DNA phenotyping faces challenges due to inconsistent terminology, limited genetic understanding, and debates over technology and models.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

Alopecia areata patients have a higher risk of blood clots.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

New mouse models help study melanocytic cells for melanoma research.

A 5-year-old girl with McCune-Albright syndrome grew abnormal hair due to the drug tamoxifen.

Most children with alopecia areata have patchy hair loss and common trichoscopic features like yellow and black dots.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

PAON shows skin patterns due to genetic mosaicism.

UV-induced autofluorescence is effective for identifying different types of alopecia.

Trichoscopy effectively helps diagnose different types of hair loss in women.

Serial trichoscopy is more reliable than the modified hair pull test for tracking alopecia areata.

DNA analysis can help tailor alopecia treatment.

Certain genes may influence hair loss differently in men and women.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.