Search

everythinglearnresearchcommunity

for

Search:↓

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

The surgical technique of scalp advancement and pretrichial brow lift shortens the forehead and lifts brows, is good for women and transgender women with high foreheads, but not recommended for men and has some risks.

Stress hormone CRF can cause hair loss by affecting hair growth cells and hormones.

Most patients with frontal fibrosing alopecia are middle-aged women, often have thyroid disease, and some treatments can help stabilize the condition.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Medical castration in prostate cancer patients can increase the risk of serious heart rhythm problems, so it's important to monitor heart activity during treatment.

Men and women have different hairline restoration needs, with natural design being more complex for women, and hairline changes being important for transgender individuals' transitions.

The CORIN gene variant causes the golden color in Siberian cats.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

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

Neurosteroids play a key role in controlling the brain-adrenal gland activity in pregnant sheep, both in normal and stressful situations.

JAK inhibitors help hair regrowth but not fully effective for androgenetic alopecia.

PCOS is a common hormonal disorder in women linked to several health risks and can be managed through various treatments.

Most Spanish Caucasian women have a widow's peak, and their hormone levels suggest they process certain hormones faster.

Some patients with Alopecia Areata experience itch due to immune cells and enzymes that cause itching.

Carlos Oscar Uebel developed a hair transplant method that looks natural, has low risk, and shows full growth in 6-12 months.

Stress may contribute to hair loss in alopecia areata by affecting immune responses and cell death in hair follicles.

Mechanical trauma like towel drying can cause knotted hair even in straight hair.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Polycystic Ovary Syndrome (PCOS) often leads to severe acne, and lifestyle changes and hormonal treatments can help manage it.

Cheap treatments for excessive hair growth in women can improve symptoms by 35-40% after one year.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.