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People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The scraggly mutation causes hair loss and skin defects in mice.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

Chromosomal differences affect how muscle cells respond to testosterone.

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.

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.

Taking Propecia might lead to the development of 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.

S100A3 protein is crucial for hair shaft formation in mice.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Certain gene variations might be linked to severe acne in women but not in men.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

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.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.