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Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Both HLA-B and MICA are independently linked to alopecia areata.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

Inflammatory acne damages skin stem cells and reduces their growth, leading to atrophic acne scars.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

Small amounts of DNA can be found in the hair shaft, especially near the root, but it decreases with hair treatments and washing.

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

The exact cause of frontal fibrosing alopecia is unknown, but it's not likely due to sunscreen.

The patient with Ankylosing Spondylitis had shoulder joint damage and bone changes.

Alopecia areata, a type of hair loss, may be passed through T cells and has genetic links, while treatments vary in effectiveness. Male pattern baldness can be treated with finasteride and is influenced by androgens in hair follicles.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

Genetic factors affecting skin health and body weight may increase the risk of dermatophytosis.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

A man had two rare autoimmune diseases that might be connected.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.

Crash dieting can cause hair loss due to severe calorie restriction.

Spheroid culture in agarose dishes improves survival and nerve cell growth in thawed human fat-derived stem cells.

New Australian advertising rules improved stem cell marketing practices but further regulation is needed for consumer safety.