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Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

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

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Alopecia areata involves immune response and gene changes affecting hair loss.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Alopecia Areata is a hair loss condition affecting all genders, often linked to other diseases, with treatments available but varying success rates.

The review highlights the need for more research on transgender dermatology, the role of dermatologists in gender affirmation, and the effects of hormone therapy on skin and hair.

Sebum production varies by individual and is influenced by age, gender, and hormones, affecting skin and hair health.

The document concludes that various treatments for skin conditions are effective, but some require further research, and certain factors like gender and lifestyle can influence disease outcomes.

Eczema and fungal infections are the most common skin problems in Japan, with different age groups and genders affected by various conditions.

Most medical students in the study had skin and hair issues, with acne, hair loss, and sun tan being common, and these issues varied by gender and origin.

Scalp massages may help stabilize or regrow hair in people suffering from hair loss, regardless of age, gender, or use of other treatments.

Acne was the most common skin problem in kids, with other conditions like warts and eczema also frequent, varying by age and gender.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Stress increases certain chemicals in the skin and nerves, which might worsen skin conditions.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

The document explains how to identify different hair problems using a microscope.