beckwith wiedemann syndrome

What Causes Beckwith-Wiedemann Syndrome?

BWS is primarily caused by changes in the imprinting of certain genes on chromosome 11. These changes can occur sporadically or be inherited. The most commonly affected gene regions are 11p15.5, which is involved in growth regulation.

Frequently asked queries:

What is Beckwith-Wiedemann Syndrome?
What are the Symptoms of BWS?
What Causes Beckwith-Wiedemann Syndrome?
How Can Parents Support a Child with BWS?
Who Conducts the Assessment?
What Information is Protected Under HIPAA?
Who Can Be a Pediatric Advocate?
What Tools and Technologies Are Used for Monitoring?
Why are Chemical UV Filters Important for Children?
Why is Resource Access Important?
What are the Implications of Variability in Pediatric Care?
What Are the Barriers to Effective Communication?
What are the Common Risks Associated with Unsafe Food?
What Should Parents Do If They Encounter a Fake Website?
How is Measles Diagnosed?
What are the Common Academic Problems in Children?
How Should Petroleum-Based Products Be Applied?
How is IBS Managed in Pediatric Patients?
What are the latest diagnostic tools for neonatal disorders?
What Are Congenital Heart Defects (CHDs)?
Follow Us
Top Searches
Nasal Obstruction Neonatal Disorders Neonatal sepsis Pediatric Anemia Pediatric Cardiovascular Diseases Pediatric Epilepsy

Partnered Content Networks

Relevant Topics