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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

Eculizumab helps reduce blood transfusions and stabilize hemoglobin but increases infection risk and is expensive.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Low androgen levels can still cause female pattern hair loss.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

DHEA reduction may be linked to frontal fibrosing alopecia, but more research is needed.

The study found that in Eclipta prostrata roots, coumestans come from acetate and shikimate pathways, and phenylpropanoid is made only through the shikimate pathway.

Cyproterone acetate is used for topical treatment of diseases dependent on male hormones.

A new genetic mutation was found causing hair and eye issues in a boy.

Researchers identified new compounds in Platycladi Cacumen and found variations in its flavonoid content, which could aid in its quality control.

ACOD1 deficiency worsens hair loss by causing cell aging and mitochondrial problems, but 4-OI may help.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Deuruxolitinib improves anxiety and depression in severe alopecia areata patients.

PNH can occur in patients with SLE, so doctors should be aware of this.

The new compound may be a safer alternative to finasteride for prostate protection.

Hair root sheaths can be used to accurately analyze genetic markers.

Prostaglandin E2 helps prevent hair loss from radiotherapy by protecting hair growth cells and aiding self-repair.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Systemic photodynamic therapy can effectively treat stubborn folliculitis decalvans with few side effects.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.