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 Can Parents Contribute to Neonatal Safety?
What are the recent advancements in car seat safety regulations?
What is Formaldehyde?
How is Vitamin K Deficiency Diagnosed?
What is the Children's Oncology Group (COG)?
How Critical are Immunizations in Pediatric Care?
What are the signs that a child may be suffering from lead poisoning?
How Does Uterine Rupture Affect Neonates?
How Can Parents Build a Strong Support System?
What is a Gyroscope?
When is MRCP Recommended?
How Can Parents Support Their Child with MRELD?
What is Enterovirus?
Follow Us
Top Searches
Nasal Obstruction Neonatal Disorders Neonatal sepsis Pediatric Anemia Pediatric Cardiovascular Diseases Pediatric Epilepsy

Partnered Content Networks

Relevant Topics