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Proper hygiene, adequate sleep, and self-care can reduce common skin diseases.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

The document says that early treatment of Acne Vulgaris is important to prevent scarring and that adult onset acne is common in women, often due to hormonal imbalances.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

*Acorus calamus* has many medicinal benefits but needs more safety research.

Not enough vitamin B6 in pregnant rats' diets caused poor development and health in their babies.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

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

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Omeprazole effectively treats severe acid reflux in children for short-term use, but long-term safety needs more research.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Hibiscus plant extracts may have health benefits like lowering blood pressure and protecting the heart.

JAK inhibitors help with skin conditions but need more research on dosing and safety.

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

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

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

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Adrenal disorders can cause lasting brain and behavior issues in children.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Leucaena leucocephala is nutritious but needs careful processing to remove toxins.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.