Search

everythinglearnresearchcommunity

for

Search:↓

The document explains the genetic causes and characteristics of inherited hair disorders.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

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.

Skin issues can indicate immune system problems.

RXRα is crucial for proper immune response and links diet to immune function.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

TGM3 is important for skin and hair structure and may help diagnose cancer.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

Androgens can both increase and decrease hair growth in different parts of the body.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Alopecia areata causes hair loss, has no cure, and various treatments exist.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.