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Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

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.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

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

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

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

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

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

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

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

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

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

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

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

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

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.

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

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

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 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.

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.

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

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

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

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.