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The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Tigason improved hair growth in a boy with monilethrix without side effects.

Whale genes show changes that help them live in water, like less hair and better flippers.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Some skin diseases and their treatments can negatively affect male fertility.

MC4R gene variants not linked to female hair loss.

Certain gene variations are linked to better memory in healthy Chinese women.

The document concludes that early diagnosis is key for treating common baldness in women, but reassurance is often the best approach as hair thinning can be a normal part of aging.

Androgens can both increase body hair and cause scalp hair loss.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The document concludes that recent studies help tell apart desmoplastic trichoepitheliomas from other skin tumors, but more research is needed for clear differentiation.

The document concludes that managing PCOS involves lifestyle changes, medication for symptoms, and weight loss for fertility improvement.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Ethylene and auxin hormones interact in complex ways that are essential for plant growth and development.

A patient grew extra hair on their ears after treatment for testicular cancer, possibly due to hormonal changes or genetics.

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

Different proteins are linked to the varying thickness of sheep and goat hair types.

Vitiligo causes white skin patches and can lead to psychological stress.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.