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A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

CMV infection increases the risk of GvHD after bone marrow transplants.

A woman with inflammatory bowel disease improved after treatment with ustekinumab for a rare skin condition associated with her disease.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Corticosteroids, especially prednisone, improve short-term muscle strength in Duchenne muscular dystrophy but have manageable side effects.

BMI is a simple, cost-effective tool for screening obesity and related diseases.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

A 13-year-old girl with various symptoms was successfully treated for autoimmune disease using the antibiotic co-trimoxazole.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Combined light therapy improves eye health and quality of life for those with meibomian gland dysfunction.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Methotrexate treatment for rheumatoid arthritis has a serious infection rate of about two per 100 patient-years.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

A man developed a skin cancer called folliculotropic mycosis fungoides after a kidney transplant.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The boy's symptoms improved with thyroid treatment, and he lost weight, but occasional palpitations persisted.

Tocilizumab therapy may cause skin and hair conditions like halo naevi, vitiligo, and alopecia areata.

Testosterone treatment in transgender teens can worsen acne, requiring careful treatment due to mental health and medication side effects.

Glucocorticoid corticosteroids improve muscle strength in Duchenne muscular dystrophy but can cause side effects.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.