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PCOS is a common condition in women that causes various symptoms and health issues, treatable with lifestyle changes and medication.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

Insulin resistance is significantly linked to a higher risk of depression in women with PCOS.

Epilepsy and certain epilepsy drugs can lead to reproductive problems in women, but changing medication might improve these issues.

Women with PCOS often have metabolic issues like insulin resistance and a higher risk of diabetes and abnormal lipid levels.

Women with PCOS often have insulin resistance, abnormal lipid levels, and a higher risk of diabetes and heart disease; lifestyle changes and medication like metformin can help manage these risks.

Hormone treatment for transsexual individuals is effective but carries risks like thromboembolic events and mood changes, with most side effects being minor and reversible.

The document concludes that treating androgen excess needs patience, managing expectations is important, and many drugs used are not officially approved, suggesting cosmetic options for mild cases.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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.

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

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Excessive body hair can signal complex health issues.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The surgery for severe congenital ptosis in children is safe and effective, with good long-term results.

Minoxidil use during pregnancy can cause excessive hair growth and multiple birth defects in the baby.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

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

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

A specific gene mutation causes congenital hair loss.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.