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People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Essential oils may help hair health but lack strong scientific proof and can cause allergic reactions.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Keratins are important for skin cell health and their problems can cause diseases.

Accurate diagnosis and personalized treatment are crucial for managing women's hair loss.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Adult female acne is complex and requires a combination of treatments for effective management.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

New skin substitutes for treating severe burns and chronic wounds are being developed, but a permanent solution for deep wounds is not yet available commercially.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

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

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

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

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

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

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

The review explains how hair products work and the science of different hair types to help improve hair care research.

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

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.

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

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

The document concludes that more standardized research is needed to understand exosome therapy's safety and effectiveness for hair loss treatment.