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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

A rare hair follicle tumor was found on a woman's vulva.

Treat limited stage small cell lung cancer with chemotherapy and radiation, and consider preventive brain radiation for better survival chances.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Abnormal activation of hair follicle stem cells and Wnt/β-catenin signaling contributes to sebaceous neoplasms.

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.

Men with low testosterone should be carefully evaluated and monitored before and during treatment.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Hair loss in postmenopausal women due to ovarian hyperthecosis is rare, but removing the ovaries can significantly improve the condition.

Buserelin safely and effectively suppresses early puberty, potentially improving final height.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

The cyst had unusual keratin spherules and resembled bone marrow.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Sonidegib often causes hair loss, and LC-OCT helps identify early signs.

Trichofolliculoma is a unique benign tumor mainly affecting middle-aged adults' faces, often misdiagnosed without histopathology.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Polypoid cystitis can mimic bladder cancer but can be effectively treated with surgery, stents, and medication.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A rare tumor caused unusual hormone production leading to Cushing syndrome.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The patient's long-term symptoms were due to Sheehan's syndrome, which improved with hormone therapy.

Immunohistochemistry helps accurately identify and differentiate malignant trichilemmoma.

Finasteride changes androgen receptor location in rat epididymis without altering tissue structure.