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Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Gonadal dysgenesis, like Turner's and Klinefelter's syndromes, negatively affects bone health, but hormone treatments can help.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Human hair follicle stem cells can turn into multiple cell types but lose some of this ability after being grown in the lab for a long time.

The four main causes of hair loss in children are fungal infections, pulling out hair, autoimmune hair loss, and stress-related hair shedding.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

The document concludes that managing side effects of MS therapies is crucial for treatment success and patient adherence.

Licorice has many traditional health benefits, but more research is needed to fully support these claims.

Fetal skin has unique immune cells different from adult skin.

N793 may improve hair density in people with mild hair thinning.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

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.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

The perception of excessive hair growth in women as abnormal is more influenced by cultural norms than by medical reasons.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Anticonvulsant drugs may cause temporary chromosomal abnormalities.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

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

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Hair loss can be linked to hormonal changes, and physical conditions like heart defects can cause depression.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

The document does not determine if adults with aphallia are fertile.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.