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Being overweight, having gallbladder removal surgery, and taking cholesterol-lowering drugs are linked to a higher chance of getting vulvar lichen sclerosus.

Lower vaspin levels in the blood may indicate a better response to fertility treatment in women with PCOS.

Imbalances in metals and proteins may help understand and treat bipolar disorder and schizophrenia.

PRP helps tissue repair but lacks standard preparation methods.

Mutations in keratin genes cause cell fragility and various skin disorders.

Treatment strategies for breast cancer affect blood health, causing issues like anemia and require nutritional counseling.

β‐thymosins, especially thymosin β4, help in heart protection, wound healing, and hair growth by stabilizing actin in cells.

Oral zinc sulphate is an effective and safe treatment for thallium poisoning.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Venous catheterization may help diagnose the cause of female hyperandrogenism when imaging is unclear.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A rare skin condition usually on the face was found on a man's heel.

Thallium poisoning can cause worsening nerve damage and vision loss without typical symptoms.

Thallium poisoning can cause severe neurological symptoms and hair loss.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Platelet-rich plasma helps heal wounds and regenerate tissue in various medical fields.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

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

People with both obvious and not-so-obvious underactive thyroid issues often have higher levels of the hormone prolactin.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A woman with both TLE and SLE improved with hydroxychloroquine treatment.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

PRF and CGF are becoming more popular than PRP in regenerative medicine due to their simplicity and lack of additives.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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