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Alopecia areata and myasthenia gravis can occur as rare symptoms of breast cancer.

A unique case of skin cancer showed unusual calcification, possibly linked to calcium-binding proteins.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

New mutations in the DSG4 gene cause a rare hair condition.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Most patients with dermatomyositis had skin rash and were treated with prednisolone and hydroxychloroquine.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Some skin lymphomas can look like common skin issues and need careful testing to diagnose correctly.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

A potential genetic link between Werner syndrome and kidney disease was suggested.

Lymphoma should be considered in unusual scalp hair loss cases, as treatment can work but may lead to severe complications.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

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

Two women were diagnosed with a rare melanoma that looked like hair loss but was actually a type of skin cancer.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

Prednisone reduces organ mast cell infiltration but does not alter the abnormal appearance of mast cells in systemic mastocytosis.

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

Membership in a self-help organization is linked to being better informed and having a higher education, but it doesn't clearly affect disease outcomes.

A woman had meningitis caused by mixed connective tissue disease, not an infection.

Different tumor cells in one basal cell carcinoma can cause mixed treatment responses, suggesting personalized treatment is needed.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

Scalp biopsies are crucial for diagnosing hair loss causes in cutaneous lymphoma patients.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.