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Some breast cancer patients developed permanent hair loss after chemotherapy and hormonal therapy, showing patterns similar to common baldness and alopecia areata.

Heat shock proteins help basal cell carcinoma grow by responding to inflammation signals.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Chemotherapy reduces splenic melanin in mice.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

Rare ovarian tumors can cause hyperandrogenism, even if imaging appears normal.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Benign ovarian tumors can cause excess male hormones and related conditions in postmenopausal women.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

A rare ear cyst contained hair fragments.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

A woman's excessive hair growth and high testosterone were caused by a rare ovarian tumor, which was successfully treated with surgery.

Women with PCOS are more likely to have fatty liver disease, especially if they have metabolic problems.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

CDK4/6 inhibitors may cause hair loss in breast cancer patients.

Deferasirox combined with sorafenib reduces liver cancer risk and lessens treatment side effects.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

BCC can protect heart cells from damage caused by oxidative stress.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Rare ovarian tumors can cause hyperandrogenism, even if imaging appears normal.