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Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Longer CAG repeats in gene linked to more severe hair loss in females.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Reduced AR gene methylation may cause early pubic hair growth in girls.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.