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New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Male pattern baldness might have evolved to help protect against prostate cancer by increasing UV radiation on the scalp.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Hypothyroidism in dogs is usually caused by immune system issues or gland atrophy, affects middle-aged purebreds most, and is treatable with medication.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.

A 28-year-old man with type 1 diabetes had skin and hair issues due to zinc deficiency.

Cinnamon bark extract may help prevent weight loss and hair loss in breast cancer patients during chemotherapy and is safe to use.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

Excessive blow-drying can cause "bubble hair," leading to hair loss and fragility, but improves when heat use is reduced.

Baldness may lower the risk of testicular cancer.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

The document concludes that while some organisms can regenerate body parts, mammals generally cannot, and cancer progression is complex, involving mutations rather than a strict stem cell hierarchy.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A thorough skin history and full examination are important for diagnosing and understanding the impact of skin diseases.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

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.

Micrografting is the most effective surgical method for permanent hair restoration.

Darker hair colors may increase the risk of alopecia areata, while lighter hair colors may decrease it.

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

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.