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A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

DHT, a testosterone byproduct, causes male pattern baldness.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

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

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Injecting platelet-rich plasma under the skin significantly improves hair growth and quality without harmful effects.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

The research found specific genes and pathways that control fur development and color in young American minks.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Janus kinase inhibitors are promising drugs for treating autoimmune and inflammatory diseases.

EDA2R gene linked to hair loss.

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.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

Using methods like lasers and microneedling with drugs can improve hair regrowth for alopecia, but more research is needed on safety and best practices.

Testosterone is crucial for development, growth, and various body functions in mammals.

L-Carnitine-L-tartrate may help hair grow and prevent hair loss.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

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

Large prostate links to more hair loss, but age of onset doesn't affect it.

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