juvenile myelomonocytic leukemia (jmml)

What are the Risk Factors for JMML?

While the exact cause of JMML is not known, certain genetic conditions increase the risk of developing this leukemia. These include:
- Neurofibromatosis type 1 (NF1)
- Noonan syndrome
- Germline mutations in the above-mentioned genes

Frequently asked queries:

What is Juvenile Myelomonocytic Leukemia (JMML)?
What are the Symptoms of JMML?
How is JMML Diagnosed?
What are the Risk Factors for JMML?
What Treatment Options are Available for JMML?
What is the Prognosis for Children with JMML?
What are the Long-term Follow-up Care Needs?
How to Assess Fluid Status in Children?
What Role Do Pediatricians Play in Managing Sulfur Dioxide Exposure?
How to Access Support Networks?
How Are Pain and Distress Managed in Neonates?
Can Parents Refuse Vitamin K for Their Newborn?
Why Use Percentiles?
How are Epigenetic Modifications Relevant to Neonatal Disorders?
How Can Pediatricians Support Special Education Teachers?
What is a Cleft Palate?
Who are Pediatric Hematologists?
Who Can Be a Pediatric Advocate?
How is Avulsion Diagnosed?
Why Use PCA in Neonatal Disorders?
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