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Topical minoxidil helps treat hair loss in teens, but more research needed for safe options.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Experts recommend using evidence-based methods to diagnose and treat hirsutism, focusing on symptoms and underlying causes.

Chemicals and body size might change when puberty starts and progresses, but more research is needed to confirm this.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Antibiotics can reduce acne but may lead to resistant bacteria, and understanding the skin's bacteria is important for treatment.

The paper concludes that the 1982 criteria for diagnosing systemic lupus erythematosus need updating to improve accuracy and involve dermatologists in the process.

Preoperative pain assessment, regional anesthesia, and vitamin C can help prevent CRPS after surgery.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Trichoscopy helps diagnose and monitor alopecia areata by looking at a combination of specific hair and scalp features.

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

Children with loose anagen hair have easily pluckable hair due to root sheath problems, and it might improve without treatment.

Choosing the right recall period for patient feedback is important for accurate data and depends on the disease, symptom changes, and patient impact.

Finasteride reduces hairiness and androgen levels in women with unexplained excessive hair growth.

The document concludes that there are no effective clinical treatments for hearing loss due to hair cell damage, but research is ongoing.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Certain hairstyles and less hair oil use in African American girls can lead to scalp conditions like traction alopecia and seborrheic dermatitis.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

FOXN1 gene variants cause low T cells and immune issues from birth.

Reduced AR gene methylation may cause early pubic hair growth in girls.

HIV can cause unusual and severe skin problems that are hard to treat.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.