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A man developed myasthenia gravis after alopecia areata, and treatment improved his symptoms and stopped hair loss.

Timely diagnosis of SLE is crucial due to symptom overlap with fibromyalgia.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Most UK dental schools don't teach non-surgical facial aesthetics, but dentists have a good knowledge base to provide these services.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

Breast cancer survivors may have a higher risk of falls, tamoxifen could prevent breast cancer and deaths, new guidelines urge caution with prostate cancer therapy, and early balding in men may indicate a higher prostate cancer risk.

ECCL should be considered in patients with specific skin and eye lesions.

Glucocorticoid corticosteroids improve muscle strength in Duchenne muscular dystrophy but can cause side effects.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

Genetic disorders can disrupt mineral and trace element metabolism, affecting health.

Surgery to fix a broken upper arm bone can sometimes lead to nerve damage.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

The girl's symptoms suggest a complex condition that's hard to diagnose despite normal test results.

The EMG-to-force model accurately predicts hip muscle forces during walking.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

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

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Type 1 diabetes patients often have other autoimmune diseases, which complicate their care.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.