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The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

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

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Antiandrogen therapy helps treat genetic hair loss.

Researchers found two new genetic variants linked to Alzheimer's disease.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Combining yoga and certain herbs can effectively manage PCOS symptoms and improve quality of life.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

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

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document is a detailed medical reference on skin and genetic disorders.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

Acne significantly affects mental health and quality of life, with research suggesting hormonal and genetic factors in its development and emphasizing early treatment to prevent scarring.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.