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The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

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

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Stress, nutritional issues, and chronic diseases can cause hair loss, and nail changes may signal internal diseases; treatment focuses on the underlying cause.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

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."

Understanding how acne develops in different diseases could lead to new treatments.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The cancer drugs bortezomib and lenalidomide cause skin side effects in many patients.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Cardiovascular drugs can cause various skin problems, so recognizing these reactions is important.

Hair changes can indicate systemic diseases or medication effects.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The document is a detailed guide on skin conditions and treatments for dermatologists.

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.

People with Down's syndrome often have more skin problems due to a weak immune system.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

Trichoscopy is a useful tool for diagnosing and managing hair and scalp conditions, often better than traditional methods.

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

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

In 2017, pediatric dermatology advanced with new treatments and insights into various skin conditions in children.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The conclusion is that there's a link between high testosterone levels, insulin resistance, and certain skin conditions, regardless of obesity.