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The herbal mix of hibiscus and vitex shows promise for treating autoimmune diseases due to its effectiveness and low toxicity.

A young boy with Netherton syndrome improved significantly using IVIG, dupilumab, and dietary changes.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

IVIG and dupilumab effectively improved symptoms in a child with Netherton syndrome.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

CUR-loaded micelles improve skin delivery and effects of curcumin for pain and infections.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Alternating treatment with two drugs could help cells in a rapid aging disease.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Gene therapy shows promise for healing chronic wounds but needs more research to overcome challenges.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

Mutations in the LIPH gene cause woolly hair in a child.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

The severity of female pattern hair loss is linked to how long someone has had it, not to levels of certain nutrients or hormones.

The hydrogels improve wound healing and tissue regeneration better than traditional treatments.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.