Search

everythinglearnresearchcommunity

for

Search:↓

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Camellia japonica extract may improve scalp health and promote hair growth.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

The document is a detailed medical reference on skin and genetic disorders.

Alopecia Areata is treated with drugs and therapies to reduce inflammation and immune response.

The conclusion introduces a new way to classify skin cysts using their shape and genetic markers.

The study found that sweat glands normally suppress immune responses, but this is disrupted in certain skin diseases, possibly contributing to their development.

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

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

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

Acne significantly affects mental health and quality of life, with research suggesting hormonal and genetic factors in its development and emphasizing early treatment to prevent scarring.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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