Search

everythinglearnresearchcommunity

for

Search:↓

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

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 concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

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

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

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Covers common skin issues in kids, their diagnosis, treatment, and need for specialist care.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Topical tacrolimus is safe and effective for skin conditions, but oral tacrolimus has serious side effects.

Advances in genetics may lead to targeted treatments for hair disorders.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

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

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

Light microscopy is useful for diagnosing different hair disorders.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

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

Psychological issues with skin problems worsen patients' lives and treatment.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Newborns with ichthyosis need specific care based on their skin type.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.