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Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

The document explains the genetic causes and characteristics of inherited hair disorders.

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.

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

The girl has a genetic hair condition causing thin hair since childhood.

The ginseng market has potential for growth and needs new products and better marketing.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases by their unique visual features.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

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

To diagnose hair loss, use a systematic approach including history, exams, and tests.

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

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

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

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Assessing newborn scalp hair can reveal important health information.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

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

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

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.

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.