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A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A child's scalp infection was caused by a fungus not previously known to do so, but it was successfully treated.

A woman's small, unnoticed adrenal mass turned out to be a rare non-Hodgkin's lymphoma, treated successfully with surgery and therapy.

Human hair follicle cells can be turned into neural stem cell-like cells, which might help treat brain diseases.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

SGK3 is essential for proper hair growth and health.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

A rare, harmless skin tumor was found on a man's nose.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The human scalp has different types of pigment cells in hair follicles with varying abilities to produce pigment.

Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

Testosterone metabolism in balding scalp cells may not be the main cause of hair loss.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

The cause and importance of misplaced oil glands in the hair follicle are not well understood.

Steroid cell tumors in the ovary are rare, can produce testosterone causing symptoms, and are mainly treated with surgery.

A woman's small ovarian tumor causing high androgen levels was missed by several scans but found during surgery.

A rare eyelid tumor was successfully diagnosed and removed, highlighting the need for careful examination.

Longer immunotherapy treatment may improve outcomes for Merkel cell carcinoma patients.

The Gsdma3 gene is essential for normal hair development in mice.

Leydig cell tumors can cause high testosterone and symptoms in postmenopausal women, and removing them improves symptoms.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Precocious puberty can signal familial adenomatous polyposis.

Ovarian steroid cell tumors should be considered in adults with hirsutism and high testosterone, with surgery as the main treatment.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Premature graying in young children can affect self-esteem, and addressing underlying health issues may reverse it.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.