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Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Human skin has multiple layers and functions, with key roles in protection, temperature control, and appearance.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

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

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Understanding fetal skin development helps diagnose congenital skin diseases.

Photobiomodulation effectively treats hair loss in dogs with black hair follicular dysplasia.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Microneedles improve drug delivery in various body parts, are safe and painless, and show promise in cosmetology, vaccination, insulin delivery, and other medical applications.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

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

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.