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BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

Female Pattern Hair Loss affects women's self-esteem and needs more research for better treatment.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

New genes found linked to balding, may help develop future treatments.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Genetic variations affecting skin structure play a key role in severe acne.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Adrenal disorders can cause lasting brain and behavior issues in children.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Use finasteride, dutasteride, and minoxidil for hair loss treatment.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Minoxidil effectively treats female pattern hair loss.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

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

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

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