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Sulfasalazine can cause severe allergic reactions leading to long-term autoimmune issues like hair loss and skin discoloration.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

The meeting presented findings on effective treatments for various pet skin conditions and insights into the immune responses of dogs with atopic dermatitis.

Skin and mucous symptoms are key for diagnosing autoimmune connective tissue diseases.

The case shows skin changes can indicate deeper health issues like insulin resistance, which are challenging to manage.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Acitretin can cause excess tissue growth and hair loss.

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

Acitretin treats severe skin conditions but requires careful monitoring due to serious side effects.

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

Anti-TNF therapy can cause a unique type of hair loss that may get better with topical treatments without stopping the therapy.

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

Inflammation damages sweat ducts, causing sweat gland injury.

The 7-month-old boy has a persistent rash that doesn't improve with typical skin treatments.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

A new treatment plan helps manage folliculitis decalvans effectively.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Some patients with severe alopecia areata developed skin darkening from their treatment, which may indicate a less effective response to the therapy.

The patient had a severe itchy rash and hair loss in the armpits.

Some skin conditions look like acne but are caused by drugs, and they usually get better when the drug is stopped.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

Psoriasis is the most common cause of erythroderma, and proper medical follow-up is crucial.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

A girl with Crohn's disease developed hair loss due to her increased medication, a rare side effect seen in some children.