Variable phenotype in a novel mutation in PHOX2B.
Rachel C LombardoElizabeth KramerJames F CnotaHemant SawnaniRobert J HopkinPublished in: American journal of medical genetics. Part A (2017)
We evaluated a family with three siblings, two of whom ages 2 years and 19 months, had long segment colonic agangliosis and anisocoria. The mother also had anisocoria. All three affected family members were mildly dysmorphic with a flat facial profile, square appearance to the face, depressed nasal bridge, and anteverted nares. Genetic testing identified a novel heterozygous mutation, c.234C>G, resulting in a premature stop codon in exon 1 of the PHOX2B gene. Screening for neural crest tumors was performed in the siblings and to date has been negative. This family supports a strong association between non polyalanine tract mutations, autonomic dysfunction, and Hirschsprung disease, but suggests mutation outside of the polyalanine tract may not dictate severe phenotype with significant respiratory compromise. A unique finding in this family is the association of congenital heart disease in two of the affected patients. These malformations may be a sporadic isolated finding or the result of environmental factors or a modifying allele. Given the association between congenital heart disease and aberrant neural crest cell development, however, findings are suggestive that congenital heart disease may be a rare feature of PHOX2B mutation which has not been previously reported.
Keyphrases
- congenital heart disease
- end stage renal disease
- early onset
- chronic kidney disease
- newly diagnosed
- machine learning
- oxidative stress
- peritoneal dialysis
- late onset
- prognostic factors
- heart rate variability
- stem cells
- heart rate
- copy number
- patient reported outcomes
- mesenchymal stem cells
- blood pressure
- transcription factor
- dna methylation
- chronic rhinosinusitis
- patient reported