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

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.

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.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Mutations in the AR gene cause hair thinning and loss.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

Certain DNA regions in alpacas are linked to fiber diameter.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

S100A3 protein is crucial for hair shaft formation in mice.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

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

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

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

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

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

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

A child with a rare vitamin D-resistant condition improved with treatment.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.