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

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Kawasaki Disease is rare and often missed in adults, who show different symptoms than children, and may benefit from early treatment.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.

Advanced hydrogel systems with therapeutic agents could greatly improve acute and chronic wound treatment.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Scientists found a gene in mice that causes early hearing loss.

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

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

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

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

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

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Systemic Lupus Erythematosus has varied symptoms and is hard to diagnose, affecting many body parts and requiring careful clinical judgment.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

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.

Genetic marker rs12558842 strongly linked to male hair loss.

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

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

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

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.