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cftr gene
What are Common Neonatal Symptoms of CFTR Gene Mutations?
The most common
neonatal symptoms
of CF due to CFTR gene mutations include:
Meconium ileus
Failure to thrive
Salty-tasting skin
Persistent cough or frequent lung infections
Greasy, bulky stools or difficulty in bowel movements
Frequently asked queries:
What is the CFTR Gene?
How is the CFTR Gene Related to Neonatal Disorders?
What are Common Neonatal Symptoms of CFTR Gene Mutations?
How is CF Diagnosed in Neonates?
What are the Treatment Options for Neonates with CFTR Gene Mutations?
What is the Prognosis for Neonates with CFTR Gene Mutations?
Are There Any Preventive Measures for CFTR Gene Mutations?
What are the Implications of Jaundice?
How do childhood illnesses affect school attendance?
What are the symptoms of hearing problems in children?
How can caregivers identify stress in children?
What Impact Do PTIs Have on Child Development?
What are the Clinical Manifestations in Pediatric Patients?
How is brain function assessed in children?
What challenges might pediatricians face in these collaborations?
What are Genomic Technologies?
How to Use ICD Codes?
How is OSA Diagnosed?
What Challenges Do Pediatricians Face?
How is GI Distress Diagnosed?
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