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A child's hair loss from alopecia areata was fully reversed in five months using diet and supplements.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Vitamin B12 deficiency can cause skin darkening and increased blood vessels, but treatment can improve symptoms.

No systemic treatment for alopecia areata has strong evidence of effectiveness.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

Blocking certain immune signals can reduce skin damage from radiation therapy.

People with alopecia areata often have lower vitamin D levels and more inflammation, suggesting vitamin D might be involved in the condition.

Vitamin D deficiency is common in people with certain types of hair loss, like alopecia areata and female pattern hair loss.

Finasteride helps improve hair growth in men with hair loss but may increase the risk of erectile dysfunction.

Zinc can help with some skin problems, but its effectiveness varies depending on the condition.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Hypothyroidism may worsen metabolic problems like insulin resistance and obesity in women with PCOS.

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.

The document recommends personalized, culturally sensitive treatments to rejuvenate the aging Asian face, focusing on natural results and specific techniques for skin, hair, and facial features.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Low vitamin D3 is not linked to different levels of thyroid hormones in people with autoimmune thyroid disease.

People with Alopecia areata often have lower Vitamin D levels, which might affect the severity of their condition.

Hair follicle stem cells reduced hair loss and inflammation in mice with a condition similar to human alopecia.