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A man's skin condition and poor diet led to a scurvy diagnosis.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Some skin symptoms, like chilblain-like lesions, can help identify COVID-19 and show how the immune system is responding.

Etanercept improved arthritis and psoriasis but caused hair loss, which healed after switching to sulfasalazine.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Erosive pustular dermatosis of the scalp can occur about 17 weeks after starting EGFR inhibitors, and early minocycline may help manage it.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

Skin problems are common in lupus, important for diagnosis, and can be triggered by sunlight.

Pediatric lichen is rare and diverse, and dermoscopy helps improve diagnosis and management in children.

Lymphangiosarcoma was confirmed in cats with specific skin symptoms using a lymphatic marker.

Machine learning can help identify biomarkers for personalized Pemphigus vulgaris treatment.

Warming hands improves blood flow in people with systemic sclerosis.

The condition is likely inherited in an autosomal-dominant pattern.

Late onset SLE has different symptoms and antibody profiles compared to young onset SLE.

Tinea faciale can be mistaken for lupus due to similar symptoms.

EPDS can cause recurring scalp sores and hair loss if not treated.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Modified superoxide dismutase may trigger an autoimmune response in alopecia areata.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.