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A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

Rituximab leads to longer remission and fewer side effects than cyclophosphamide.

Cyclophosphamide helped 59.4% of children with steroid-resistant nephrotic syndrome but caused side effects in 40.6%.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

A man developed autoimmune issues after a transplant, improved with treatment, but died from leukemia relapse.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

COVID-19 vaccination may trigger lupus in some people.

The girl's swelling and skin issues improved with fluid restriction and diuretics.

Post-steroid panniculitis is now rare because doctors taper steroids more carefully.

Myasthenia gravis can affect both motor and non-motor systems due to immune system issues.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Early balding in men is linked to metabolic syndrome, so screening is important for prevention.

PCOS is linked to diabetes and insulin resistance, and managing AGEs may help treat related symptoms.

Breathing in high levels of certain air pollutants significantly increases women's risk of developing Polycystic Ovary Syndrome.

Adrenal disorders can cause lasting brain and behavior issues in children.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Hormone imbalance is linked to Hidradenitis Suppurativa, a skin condition, and treatments like anti-androgenic therapy and metformin can help. It's also suggested to check patients for insulin resistance and Polycystic Ovary Syndrome.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The conclusion is that endocrinology significantly impacts medicine with various common medications used for treatment.

Aldesleukin can treat certain cancers and increase HIV patient CD4+ counts but often causes severe side effects.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Vitamin D may help reduce antibody levels in men with autoimmune thyroiditis and early-onset androgenic alopecia, but has no significant impact on thyroid function.

Anti-SSB antibodies are useful for diagnosing systemic lupus erythematosus and are linked to specific symptoms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.