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Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Metformin helps with menstrual cycles and insulin levels in PCOS but is less effective for hair growth, diabetes prevention, and weight loss, and may improve fertility and reduce diabetes risk.

Procyanidin B-2 is safe to use on skin as a hair growth product.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Finasteride can reduce fertility in some men, but stopping it increases sperm count.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

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

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

There are effective treatments available for baldness.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

PFS and PSSD are similar conditions with persistent sexual dysfunction after stopping medication.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Assessing newborn scalp hair can reveal important health information.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.