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Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Oral valganciclovir improved a patient's skin condition caused by immunosuppression.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The document concludes that DAB389-IL2 is promising for treating refractory cutaneous T-cell lymphoma, but more research is needed on its effectiveness and side effect management.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

The authors' correct affiliation is "The First School of Clinical Medicine, Southern Medical University, Guangzhou, China."

The new chemotherapy combination for advanced lung cancer showed a 35.7% response rate but caused significant side effects.