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The conclusion is that a certain test might help find cancer spread in lymph nodes for melanoma patients, but more research is needed due to false positives.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Kids with alopecia areata may experience more stress but not necessarily feel more anxious or depressed than others.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Hair proteins have weak spots in their α-helical segments.

Dihydrotestosterone (DHT) stops hair growth in mice by lowering a growth factor important for hair.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

New treatments targeting specific genes show promise for treating keratin disorders.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The circadian clock affects skin stem cell behavior, impacting aging and cancer risk.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Longer CAG repeats in gene linked to more severe hair loss in females.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

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

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

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

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Many patients on new leukemia drugs had mild to moderate skin reactions.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.