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A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Frontal fibrosing alopecia can occur with lichen planus pigmentosus, needing careful diagnosis and treatment.

Some women with Frontal Fibrosing Alopecia also have Lichen Planopilaris, which can lead to more symptoms and affect hair outside the scalp.

A girl with a rare skin condition improved after one month of treatment with acitretin.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Lupus enteritis is a rare but serious gut inflammation in lupus patients, often hard to diagnose without prior lupus symptoms.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

The LMNA mutation affects skin structure even in asymptomatic carriers.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

The painting may show signs of lupus, like a butterfly-shaped rash.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

Dilated pupils can be an early sign of HIV/AIDS.

Careful histologic examination is crucial to differentiate types of bullous lesions in cutaneous lupus erythematosus.

The horse had a rare disease causing weight loss and skin issues, leading to euthanasia due to poor treatment options.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

Aggressive SLE treatment helped hair regrowth and improved oral plaque, but scalp lesions stayed.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A 22-year-old with multiple autoimmune diseases needs a multidisciplinary treatment approach.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Early recognition and a multidisciplinary approach are crucial for effectively managing complex autoimmune conditions like SLE with CAPS and AHA.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

High doses of tryptophan may cause eosinophilic fasciitis.