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Alopecia is common in severe cases of autosomal recessive congenital ichthyosis.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

A woman with both TLE and SLE improved with hydroxychloroquine treatment.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Excessive sun protection might contribute to frontal fibrosing alopecia.

Alopecia areata can show unusual red-dotted vessels and dithranol treatment may mask typical patterns.

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

A 7-year-old dog with a rare autoimmune disease was euthanized due to severe anemia and poor prognosis.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Access to JAK inhibitor therapy for alopecia areata patients is difficult, especially for racial minorities.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

Mesenchymal stem cells from laser-assisted liposuction are as effective and safe as those from conventional methods for cell therapy.

Ritlecitinib is safe and well-tolerated for treating alopecia areata in patients aged 12 and older.

Hair regrowth was seen in 83% of children with alopecia, immune system plays a role in the condition, and various treatments showed effectiveness for hair and nail disorders.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Frontal fibrosing alopecia causes hair loss at the front hairline, and no effective treatment exists.

Corneal cells can potentially revert to stem cells, aiding in repair and regeneration.

Hair casts on the scalp may be a sign of ongoing pemphigus vulgaris and could suggest a need to adjust treatment.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

AA patients with comorbid conditions face more severe hair loss and need specific treatments.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Similar treatments might work for different types of scarring hair loss.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

LC-OCT is a useful noninvasive tool for diagnosing and monitoring alopecia areata.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.

Black women with CCCA are more likely to have uterine fibroids.