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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Intralesional therapy for keratoacanthoma is effective and has fewer side effects than systemic treatments.

Keratoacanthomas on lips may originate differently than those on skin.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

JAK inhibitors may help treat alopecia areata in children, but their safety needs careful evaluation.

Early diagnosis and treatment are crucial for CAPS, and Eculizumab can be effective.

Dermoscopy helps diagnose rare GLPLS in males.

Mogamulizumab can cause hair loss and skin rashes.

Most lupus patients in coastal Kerala had skin-specific lesions that could help diagnose the disease, and non-specific skin issues were linked to more severe, systemic lupus.

Fungal infections should be considered in scalp swelling to avoid misdiagnosis.

Digital gangrene can be a rare first sign of late-onset systemic lupus erythematosus.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Many survivors of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Togo suffer long-term eye and skin problems.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

A child with a rare scalp condition regrew hair after treatment.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

Timely diagnosis and aggressive treatment with high-dose steroids and B-cell depletion therapies are effective for severe acute cutaneous lupus.

Systemic lupus erythematosus is a chronic disease causing inflammation and various symptoms, mainly in young women, treated with anti-inflammatory and immunosuppressive drugs.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

A young woman with kidney cancer experienced rare hair loss from a cancer drug and unusual cancer spread, suggesting early drug treatment might reduce spread and prolong survival.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

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