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Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

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

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

In vivo reflectance confocal microscopy is useful for evaluating hair shaft diseases but needs improvement for deeper hair follicle issues.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

Neuroactive steroids and the enzyme 5α-reductase might be involved in the development of Tourette's syndrome.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A mutation in mice causes hair loss and immune problems.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

New genes linked to woolly hair have been found, which could help treat it and change hair texture.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Skin patterns are formed by simple reaction-diffusion mechanisms.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Vitiligo and alopecia areata may share common causes.

New treatments like nanotechnology show promise in improving skin cancer therapy.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

The document concludes that more research is needed to fully understand the causes of PCOS.

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

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.