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Some drugs can cause skin, nail, and hair problems, which are important for healthcare professionals to recognize and report.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Irregular menstrual cycles in exercising women may be linked to energy deficiency or hormonal imbalances, requiring careful diagnosis for proper treatment.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The document explains the genetic causes and characteristics of inherited hair disorders.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

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

PRP shows promise for treating female hair loss but needs more research.

Nanofat grafting improves scars, rejuvenates skin, and may help hair growth safely, but more research is needed.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Quercetin effectively treated and prevented hair loss in mice.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Alopecia areata involves immune activation in the scalp, suggesting treatments targeting TH1, TH2, and IL-23 pathways.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

ACTH may be an effective first-line treatment for acute calcium pyrophosphate crystal arthritis.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The document explains how the male reproductive system works, its role in making testosterone, and how conditions like obesity can disrupt it, leading to low testosterone and fertility issues.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.