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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A male with aromatase deficiency improved bone health with estradiol treatment.

Early diagnosis and treatment of TPP can prevent complications.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

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

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Teriflunomide is effective and generally safe for treating relapsing-remitting multiple sclerosis.

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

Doctors have known about fungal skin infections for a long time, but only made major progress in understanding and treating them since the mid-1800s.

Daughters of women with PCOS generally experience normal puberty but may have more body hair and different body fat distribution.

Diphencyprone treatment increases CD8 lymphocytes in the scalp, which is associated with hair regrowth in alopecia areata patients.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

The document concludes that supportive home environments and addressing parent-child interactions can effectively treat trichotillomania in children.

Acitretin is effective for severe psoriasis and can be used long-term due to no immunosuppression, but must be carefully monitored for side effects and is not for pregnant women.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Gene linked to common hair loss found, may lead to new treatments.

Early diagnosis and aggressive treatment are crucial for better outcomes in lymphomatoid granulomatosis.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Coating surfaces with human hair keratin improves the growth and consistency of important stem cells for medical use.

Minoxidil 2% effectively treats Monilethrix without side effects.

The hepatitis B vaccine did not cause hair loss in the tested mice.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

Family members of North Indian women with PCOS have a high rate of metabolic syndrome.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Anabolic steroid users may face higher risk of severe COVID-19.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.