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The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Using special RNA to target a mutant gene fixed hair problems in mice.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

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.

Chemotherapy can cause significant hair thinning and changes in hair texture, while tamoxifen has a smaller effect.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Future hair cosmetics will be safer and more effective.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

The document is a detailed medical reference on skin and genetic disorders.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

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

The conclusion is that an algorithm using trichoscopy helps diagnose different types of hair loss but may need updates and a biopsy if results are unclear.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Caffeine may help hair growth in hereditary hair loss.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

Finasteride solution helps treat hair loss.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.