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Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Canine hair follicles have stem cells similar to human hair follicles, useful for studying hair disorders.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Hair loss requires customized treatments based on its various causes and types.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

The document concludes that more research is needed to fully understand the causes of PCOS.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.