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An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

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

New genetic mutations linked to rare skin disorders were found in three newborns.

Some skin medications can harm male fertility, but they don't seem to cause birth defects from father's exposure.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

High levels of anti-Müllerian hormone can indicate polycystic ovarian syndrome in women who can have babies.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

High levels of androgens during early development may cause PCOS-like symptoms.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Weight loss and metformin don't significantly change vaspin levels in women with PCOS.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Metformin helps with menstrual cycles and insulin levels in PCOS but is less effective for hair growth, diabetes prevention, and weight loss, and may improve fertility and reduce diabetes risk.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Histone modification is key in treating chronic inflammatory skin diseases.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.