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Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

Cortisone reductase deficiency can cause high androgen and cortisol levels and may be missed in women with similar symptoms.

The man's symptoms improved and the tumor shrank after treatment with cabergoline.

These ovarian conditions cause high testosterone levels.

Low-dose chemotherapy is safer, more effective, and cost-effective than surgery for treating bone lesions in children.

Lavender oil use in a child may be linked to early puberty signs and elevated tumor marker levels.

Removing both ovaries treated the woman's excess male hormone symptoms.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

An 86-year-old man with prostate cancer was diagnosed with a rare, low-grade breast cancer and underwent surgery but declined additional hormone therapy.

Somatic BHD mutations are rare in Japanese renal tumors.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

A rare scalp tumor involving two hair follicles was successfully removed with surgery, with no recurrence after 7 months.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

A man had four testicles, two of which were outside the scrotum and looked like fatty lumps.

Pre-surgical embolization and a two-stage resection improve outcomes for rare sacral tumors.

Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

Men with liver cancer have higher levels of a specific testosterone byproduct in their liver and blood, despite overall lower male hormone levels.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.

Adrenocortical carcinoma is a rare, aggressive adrenal gland cancer with a poor outlook.

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

Dihydrotestosterone (DHT) promotes the growth and spread of aggressive brain tumor cells.

Increased ODC activity leads to skin tumors by recruiting stem cells, not by toxic byproducts.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

ACTH-dependent Cushing's syndrome linked to metastatic cervical cancer is rare and has high risks.