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Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

The exact cause of increased 5α-reductase activity leading to hirsutism in women is still unknown.

Stress and emotional factors can worsen skin conditions by affecting the immune system.

The document concludes that sexual and psychiatric side effects from 5-alpha-reductase inhibitors are reported, but more high-quality research is needed to understand how often they occur.

Testosterone therapy seems safe and effective for transgender men with proper care, but more long-term research is needed.

Hair can indicate early signs of metabolic disorders, with issues like protein deficiency stopping hair growth.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Betamethasone can effectively treat alopecia areata.

Higher DHT in male baldness may protect against prostate cancer.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Where a rhesus macaque used to live can affect its chances of getting alopecia later in life, and females are more likely to be affected than males.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Early onset, severe types, nail changes, family history, and body hair loss worsen alopecia areata prognosis; sticking to treatment helps.

Hair quality is genetically determined and linked to its composition and strength.

The research identified proteins that change as goat hair follicles begin to form, helping to understand how cashmere grows.

The document concludes that effective acne treatment requires a personalized combination of therapies and long-term commitment, with retinoids being important for maintenance.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Male and female hair loss have different genetic causes.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

The skin's bacteria might influence the development of a hair loss condition called alopecia areata.