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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

SLE is more common among Nigerians than previously thought, especially in women, requiring early treatment.

Graham-Little syndrome causes hair loss and skin bumps, with difficult treatment options.

Sulfasalazine can cause severe allergic reactions leading to long-term autoimmune issues like hair loss and skin discoloration.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

Oral ulcers are common in SLE patients and often link to other symptoms.

A woman with Lupus Vasculitis improved after treatment with steroids and other medications.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

The man was diagnosed with lupus and improved with treatment.

A 16-year-old girl with lupus symptoms improved with treatment despite negative ANA tests.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

Certain skin symptoms can help detect and manage systemic lupus.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Early recognition and treatment of SLE can improve outcomes in patients with complex symptoms.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

The 2012 criteria are better for diagnosing atypical lupus cases.

COVID-19 may trigger systemic lupus erythematosus, requiring careful diagnosis and treatment.

A patient with both bullous lichen planus and systemic lupus erythematosus showed improvement with treatment.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

A Nigerian teenager was diagnosed with neuropsychiatric lupus, showing various severe symptoms and abnormal lab results.

A young woman with lupus was treated with hydroxychloroquine and prednisone.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.