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Doctors used a special blood sampling technique to diagnose a woman's rare ovarian tumor that was producing male hormones.

Leydig cell tumors can cause high testosterone in women and are treated by removing the ovaries.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Consider rare forms of CAH for accurate diagnosis and treatment.

IL6 is linked to higher risk of heart disease in people with a certain mouth condition.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

A man had two rare autoimmune diseases that might be connected.

Men with advanced liver disease and high oestrone and low testosterone levels have worse health outcomes.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

SHBG binding properties are unchanged in male liver cirrhosis patients.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

High-dose vitamin D and an anti-inflammatory diet may help improve symptoms in autoimmune conditions like SLE and AA.

The man's skin condition improved with sun protection and topical steroids, but UV exposure still caused flare-ups.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Dihydrotestosterone boosts inflammation in fat cells more than testosterone.

Finasteride use may be linked to rare testicular tumor, but more research needed.

Taking oral contraceptives while on isotretinoin may increase the risk of high triglyceride and cholesterol levels.

People with androgenetic alopecia have a higher risk of heart disease.

A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

A rare ovarian tumor was found in a young woman with a genetic fat disorder.

Lipocalin-2 levels are higher in women with PCOS and may indicate insulin resistance.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

Statins significantly reduce testosterone and improve skin symptoms in women with PCOS.

Certain health factors can worsen fertility treatment results in women with PCOS.