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A new skin disease in four Labrador retrievers responded well to immunosuppressive treatment.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Women with low SHBG levels and a high 3a-diol G to SHBG ratio are likely to experience female pattern baldness, possibly due to a slight excess of androgens affecting sensitive hair bulbs.

Early diagnosis and treatment of PCOS in young people is important to prevent long-term health problems.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Tiny pollution particles called PM2.5 can harm skin cells by causing stress, damage to cell parts, and cell death.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Angora goat hair grows faster and produces more protein than cashmere goat hair, and certain hormones and nutrients positively affect hair growth and protein synthesis.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Eating 500 fewer calories a day and making lifestyle changes can improve PCOS symptoms and reduce diabetes risk; more research is needed on its causes and treatments.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

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.

Alopecia areata in infants may be more common than previously thought.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.