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Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Six genetic conditions are often linked to complete scalp hair loss in children.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Two mouse mutations cause similar hair loss despite different skin changes.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

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.

Six new hair loss factors in men not linked to female hair loss.

No link found between new male baldness genes and female hair loss.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Male pattern baldness involves genetics, hormones, and needs better treatments.

DHT, a testosterone byproduct, causes male pattern baldness.