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Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

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.

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

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

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

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

Early diagnosis and treatment are crucial for managing alopecia areata, morphea, and psoriasis.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Many people with hair loss had low iron and ferritin levels.

Aromatase gene variation may increase female hair loss risk.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.