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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.

Women with Systemic Lupus Erythematosus should have closely monitored pregnancies and avoid certain medications to improve their pregnancy outcomes.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

Natural herbal compounds might treat certain medical conditions by reducing DHT levels, but more research is needed to confirm their effectiveness and safety.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Finasteride safely treats hair loss without harming hormones or reproduction, but may slightly reduce sexual function.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

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.

The first pediatric case of naevus trichilemmocysticus was documented.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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

Testosterone is crucial for development, growth, and various body functions in mammals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

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

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.

Men with low or no sperm count have lower salivary testosterone levels, and saliva testing can measure their testosterone well.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.