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CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Women with PCOS and polycystic ovaries have higher male hormone levels and more insulin resistance, especially if they are overweight.

Tofacitinib may slow hair loss in scarring alopecias but is unlikely to regrow significant hair.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

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

PCOS is a complex disorder in women that can lead to various health risks and requires personalized treatment.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

Skin grafts on mice can cause an immune response leading to hair loss, useful for studying human hair loss conditions.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Baldness caused by male hormones in female-to-male transsexuals doesn't increase the risk of heart disease.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

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

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Diagnosing PCOS in teenagers should focus on signs of excess male hormones and not rely solely on ovarian ultrasound or irregular periods, and should be reassessed in adulthood.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Scientists have created a method to deliver specific cells that can regenerate hair follicles, potentially offering a new treatment for hair loss.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

ADM scaffolds help skin heal by promoting a healing-type immune response.

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

Certain drugs change freshwater snail shells to a "banana" shape.