Search

everythinglearnresearchcommunity

for

Search:↓

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Dogs could be good models for studying human hair growth and hair loss.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Gamma rays did not change hair follicle density but increased white and hypopigmented hairs in mice.

Finasteride and Dutasteride can improve hair growth in male baldness but may cause temporary sexual dysfunction and possibly affect fertility.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Using hair loss drugs finasteride and dutasteride may cause sexual side effects.

Clomipramine may significantly reduce hair-pulling in Trichotillomania, but more research is needed on treatments and early onset cases.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Goat hair shows changes in metal levels and stress when goats move from indoors to mountain pastures.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Most inconsolable crying in infants is not due to a serious cause, and a detailed check-up is typically enough to find the reason.

Hair's internal fibers are arranged in a pattern that doesn't let much water in, and treatments like oils and heat change how much water hair can absorb.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Iron deficiency might be linked to hair loss, but more research is needed.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The document provides a comprehensive index of medical and surgical topics, including hair removal, hair restoration, and various treatments for injuries and conditions.

Proper education can prevent traction alopecia in women of color.

The document covers all aspects of plastic and reconstructive surgery, from basic techniques to specific procedures for various body parts.