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

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

Ichthyoses are genetic skin disorders that affect the skin's barrier function.

Low protein diets cause severe health issues in rats, but high protein diets can reverse these effects.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

One cat with low thyroid hormone had growth issues, and another with high thyroid hormone had skin problems; both got better with treatment.

The book is a comprehensive resource on hair disorders, but lacks information on some conditions.

Malnutrition severely harms growth and development in young baboons.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

The book is a comprehensive and current guide on hair disorders, with minor flaws.

Anabolic steroids can build muscle and strength but have risks and need more research on their clinical benefits and side effects.

Noni fruit extract, specifically the FEA-3 sub-fraction, can increase hair growth and reduce baldness in male rabbits, potentially acting like common hair loss treatments.

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

Zinc can help with some skin problems, but its effectiveness varies depending on the condition.

Melatonin helps hair grow by activating a specific signaling pathway.

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.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Premature aging increases the risk of immune problems and autoimmune diseases.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Zinc can be a helpful secondary treatment for certain skin conditions, but more research is needed to guide its use.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

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

The document concludes that different types of hair loss have specific treatments, and early diagnosis is crucial for preventing permanent hair loss.

Corticosteroids, especially prednisone, improve short-term muscle strength in Duchenne muscular dystrophy but have manageable side effects.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

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.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.