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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.

Bicalutamide may help treat female pattern hair loss.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

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.

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.

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

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.

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.

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

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

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.

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

Mutations in the AR gene cause hair thinning and loss.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.