Gain professional knowledge about facial palsy treatment and its genetic nature.

The Genetic Causes of Facial Paralysis and the Importance of Psychological Care

Pediatric Wilms tumor may have a genetic component, and surgical treatment should be initiated promptly after diagnosis.

Treatment and Genetic Issues Related to Pediatric Cerebral Palsy

Understanding the genetic nature of hypophosphatemic rickets and the importance of prenatal examinations

Mental illness may have a genetic predisposition, but the mode of inheritance is uncertain.

Explore the genetic aspect of pediatric cerebral palsy, offering professional medical insights to help parents understand the causes of the disease.

Pediatric epilepsy disease can be caused by various factors, including genetics and environmental elements

Pediatric nephrotic syndrome is caused by various reasons and factors leading to increased permeability of the glomerular basement membrane, resulting in a significant loss of protein from the blood into the urine. The main clinical diagnostic symptoms include 1) marked edema: a concave swelling that typically starts from the eyelids and gradually spreads throughout the body; 2) large amounts of proteinuria: the child’s urine has an excessive amount of foam; 3) most kidney disease syndromes do not have obvious symptoms, but about 30% of pediatric nephrotic syndrome cases are primary, with the main inflammation being an increase in glomerular basement membrane permeability. Clinical diagnosis often shows a series of symptoms, including large amounts of proteinuria, low albuminemia, hypercholesterolemia, significant concave edema, and renal dysfunction.

The formation of pediatric cerebral palsy may be related to genetics, with the focus of treatment being early detection and active intervention.