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Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Immune cells are essential for early hair and skin development and healing.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

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.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Women look young for their age due to larger lips, less sun damage, and genes that prevent gray hair and wrinkles.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

New genetic locations explain much of hair color variation in Europeans.

Effective hair loss treatment in women requires correct diagnosis and can include medications like minoxidil, antiandrogens, and treatments for underlying conditions like PCOS.

Aromatase gene variation may increase female hair loss risk.

Some hair loss can be treated, especially in women due to nutrition, but some types remain untreatable.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

People with Major Depressive Disorder have a higher chance of getting Alopecia Areata, and vice versa; antidepressants may lower this risk.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.