Search

everythinglearnresearchcommunity

for

Search:↓

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concluded that FDA-approved treatments like minoxidil and finasteride are effective for hair loss, while the effectiveness of natural remedies and other non-approved treatments is not well-supported by evidence.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Skin aging reflects overall body aging and can indicate internal health conditions.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Alopecia areata causes patchy hair loss and has no cure, but treatments like corticosteroids and minoxidil can help.

Genetic testing for EGFR mutations is crucial in similar cases.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

New genetic discoveries in alopecia areata could lead to better treatments.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Different types of Armillaria fungus have a high genetic variety when partnering with Polyporus umbellatus mushrooms in China.

New genetic insights have improved understanding of hair loss, leading to a new test and treatments, but more research is needed on the test and laser comb effectiveness.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

The document concludes that effective acne treatment requires a personalized combination of therapies and long-term commitment, with retinoids being important for maintenance.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Knocking out certain genes in mice helps understand skin and hair growth problems.