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Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Sheep wool follicles absorb different amino acids at various rates and locations, which could affect wool growth based on diet and genetics.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Over 40% of postmenopausal women experience hair loss, with treatments aiming to stop further loss and possibly thicken hair.

The study concluded that combination therapy with topical corticosteroids and hydroxychloroquine or finasteride is effective in treating Frontal fibrosing alopecia in Asians.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

Some people with pattern hair loss may also have scalp inflammation and scarring similar to lichen planopilaris.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

Baldness, especially at the front, may lower the risk of testicular cancer by 31%, but its link to prostate cancer is unclear.

Obesity increases the risk of developing polycystic ovary syndrome, and weight loss can improve the condition.

Keratins are crucial for cell structure, growth, and disease risk.

Androgenetic alopecia causes hair thinning due to increased androgen activity, treatable with minoxidil and finasteride.

Higher testosterone levels can increase the risk of certain diseases like type 2 diabetes in women and prostate cancer in men, but can also protect against autoimmune diseases and hair loss. It also affects body fat and bone density.