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The combined treatment effectively managed severe skin issues in Olmsted syndrome.

Pododermatitis in farmed mink is likely caused by an unknown infectious agent with secondary bacterial infection.

Mini punch grafts effectively healed a large ulcer in a child.

Retinoids might cause temporary hyperthyroidism in some patients.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Lupus severely affects daily life, work, and mental health, with many experiencing frequent flares and medication side-effects.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A rare skin condition usually on the face was found on a man's heel.

Scalp fungal infections need oral antifungals, while other skin fungal infections can be treated with creams; keep areas dry and don't stop treatment early.

Posaconazole is a promising new treatment for toenail fungus.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Self-care strategies, especially diet and lifestyle changes, help manage cancer treatment symptoms.

Indinavir can cause hair loss and other skin problems.

Some patients using cold caps to prevent hair loss from chemotherapy got mild scalp injuries similar to frostbite.

Physical inactivity is a primary cause of many human illnesses.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Early intervention and protective measures are crucial for managing CIPA due to the lack of pain and standard treatment.

A specific gene mutation causes Olmsted syndrome.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Thyroid disease can cause skin and hair changes, treatable with levothyroxine.

COVID-19 can cause various skin issues in children, mostly not severe, with chilblain-like lesions being common, especially in adolescents.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Dr. Marina Kovalevsky and her daughter were hospitalized for suspected politically motivated thallium poisoning in Moscow.