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Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Eating isoflavone can help mice grow hair by increasing a growth factor.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Birth control pills increase the risk of blood clots, especially within the first year and with certain types.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

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.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Hair grays due to oxidative stress and fewer functioning melanocytes.

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

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

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.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

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

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Tamoxifen caused hair loss in a 52-year-old woman.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Skin cells called dermal fibroblasts are important for skin growth, hair growth, and wound healing.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.