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Creating specific biological indicators is important for early detection and treatment of PCOS.

Male pattern baldness may increase COVID-19 severity risk.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

PCOS in teens is hard to diagnose, linked to genetics and lifestyle, and managed with weight loss and medication.

Early detection and treatment of PCOS in teenagers is important to manage symptoms and prevent severe issues.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The study found that women with PCOS have more and larger ovarian follicles and differences in ovarian structure, but these features alone can't always diagnose PCOS.

Elastin staining helps assess late-stage scarring alopecia but is not definitive, and clinical diagnosis is still crucial.

The research found that MRI and certain hormone levels can help tell apart ovarian tumors from hyperthecosis in postmenopausal women, but tissue analysis is still needed for a definite diagnosis.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Polycystic Ovary Syndrome (PCOS) in teenagers is a complex condition linked to genetics and environment, often associated with obesity and insulin resistance, and is treated with lifestyle changes and medication.

Frontal fibrosing alopecia and androgenetic alopecia may be related, with a possible shared cause.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The vellus index is a simple, quick, and reliable method to assess and monitor hair growth, especially in hirsutism.

TGF-alpha is present in sheep and ferret skin and may affect hair growth without directly stimulating cell proliferation.

Scarring hair loss found in female pattern; biopsy needed for diagnosis.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.

Topical tofacitinib cream may help treat certain hair loss conditions with fewer risks.

Hair cortisol and cortisone levels may affect how work stress influences depression in Chinese fishermen.

3α, 17β-androstanediol-glucuronide is not a useful marker for androgen excess but may help monitor certain treatments.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Bullous pyoderma gangrenosum can develop on cesarean scars and may require steroids for treatment.