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Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Severe menstrual issues in PCOS women signal higher risk for heart and metabolic problems.

Pulsed electric field treatment may help the immune system fight liver tumors.

Local inflammation worsens autoimmune skin conditions by increasing antibody buildup.

Men with better urinary symptoms have a lower risk of death.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Primary amenorrhea and delayed puberty in females can be diagnosed and managed effectively.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

High doses of cyproterone acetate are linked to an increased risk of developing meningioma.

DM and AA may share a common cause.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Using PBMT and Respiro Mirtol forte after septoplasty reduces pain and inflammation.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

A rare skin condition affected only the facial hair of a 46-year-old man.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Lichen Planopilaris in teens is rare, often misdiagnosed, and responds well to steroids.

Some patients fail bladder function tests due to lower flow rates and higher remaining urine volumes, but the exact reasons for failure are unclear.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.