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Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

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

Some treatments work for common baldness, but there's less evidence for other hair loss types, and more research is needed.

Type I interferons play a key role in the development of various skin diseases.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Meis1 is crucial for skin health and tumor development.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Ozone therapy might improve cancer treatment and reduce its side effects.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

Finasteride can cause sexual problems and depression in young men.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.