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People with weakened immune systems, like those with SLE, are at higher risk for TB.

Dermoscopy helps diagnose syphilitic alopecia, and treatment with penicillin can regrow hair.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Certain skin symptoms can help detect and manage systemic lupus.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Hair and wool have complex microscopic structures with microfibrils and varying cystine content.

COVID-19 infection rates were low in patients with immune diseases, regardless of their treatment type.

A man with skin and hair symptoms improved partially with specific treatment.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Certain skin rashes can indicate COVID-19 severity, with chilblains-like rashes linked to milder cases and livedoid patterns to more severe cases.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Hair shaft abnormalities can help distinguish mycosis fungoides from other skin conditions.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

Follicular dystrophy in immunocompromised patients may be linked to medication or viral factors and can improve with treatment changes.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

Polarized microscopy helps identify hair irregularities in genetic disorders.

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

PAON shows skin patterns due to genetic mosaicism.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Infliximab improved skin and bowel symptoms in Crohn's disease but caused side effects and the disease returned after stopping treatment.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Devon Rex cats with skin issues were successfully treated with antifungal medication.

Frequent hairdryer use may worsen hair fragility in people with Pili Annulati.