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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.

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.

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

A new gene variant causes glucocorticoid resistance in a mother and son.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Enzymes called 5α-reductases have many body functions and need more research to safely use inhibitors.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

BB4CMU rice bran oil may help treat hair loss and gray hair.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

Different nail disorders are treated by targeting their specific causes and using appropriate medications or protective measures.

Six genetic conditions are often linked to complete scalp hair loss in children.

The document concludes that managing PCOS involves lifestyle changes, medication, and monitoring for associated health risks.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Using special RNA to target a mutant gene fixed hair problems in mice.

Horizontal scalp biopsy sections are better for diagnosing alopecia areata, showing fewer hair follicles and more miniaturized hairs.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Different hormones affect hair growth and conditions, with some causing hair loss and others promoting it.

The document concludes that new treatments are needed to better manage acne and reduce side effects related to current therapies.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A specific gene mutation causes Olmsted syndrome.

Polycystic ovary syndrome costs the U.S. over $4 billion a year, mainly from treating related health issues.

A new gene mutation causes insulin resistance in a girl and her mother.

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.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.