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Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Removing the thymoma improved the man's autoimmune conditions.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

5-alpha-reductase inhibitors may cause a low incidence of erectile dysfunction that decreases over time.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Fibrosing alopecia in a pattern distribution is a hair loss condition often confused with other types, requiring early treatment but usually not resulting in significant hair regrowth.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Young women with high male hormone levels or PCOS often feel more psychological distress and have a lower quality of life.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Hair loss in elderly women is often caused by various factors, including hormonal changes after menopause.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that managing hirsutism involves identifying the cause, using a scoring system for severity, combining cosmetic and medical treatments, encouraging weight loss, and providing psychological support, while noting the need for more research on drug treatments.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

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

Alopecia areata is an autoimmune hair loss condition treated with corticosteroids, and histologic confirmation is the best diagnosis method.

Hair loss in teenagers is hard to treat and lacks a cure, with some treatments available depending on the type of hair loss.

Minoxidil use during pregnancy may cause fetal harm.

Girls with PCOS during adolescence have a higher risk of developing type 2 diabetes, and early treatment can help manage this risk.

The document concludes that understanding the anatomical changes of the ageing face is important for effective rejuvenation treatments.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Early hair loss may indicate prostate issues.

There is no significant link between male pattern baldness and insulin resistance.

Most hair loss can be diagnosed with patient history and physical exam, and a few common types make up most cases.

COVID-19 can cause skin issues like chilblains and rashes, which may help in early detection, especially in patients without other symptoms.