Phenotype analysis impacts testing strategy in patients with Currarino syndrome

G. Cuturilo, J. C. Hodge, C. K. Runke, E. C. Thorland, M. A. Al-Owain, J. W. Ellison, D. Babovic-Vuksanovic

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Currarino syndrome (OMIM 175450) presents with sacral, anorectal, and intraspinal anomalies and presacral meningocele or teratoma. Autosomal dominant loss-of-function mutations in the MNX1 gene cause nearly all familial and 30% of sporadic cases. Less frequently, a complex phenotype of Currarino syndrome can be caused by microdeletions of 7q containing MNX1. Here, we report one familial and three sporadic cases of Currarino syndrome. To determine the most efficient genetic testing approach for these patients, we have compared results from MNX1 sequencing, chromosomal microarray, and performed a literature search with analysis of genotype-phenotype correlation. Based on the relationship between the type of mutation (intragenic MNX1 mutations vs 7q microdeletion) and the presence of intellectual disability, growth retardation, facial dysmorphism, and associated malformations, we propose a testing algorithm. Patients with the classic Currarino triad of malformations but normal growth, intellect, and facial appearance should have MNX1 sequencing first, and only in the event of a normal result should the clinician proceed with chromosomal microarray testing. In contrast, if growth delay and/or facial dysmorphy and/or intellectual disability are present, chromosomal microarray should be the first method of choice for genetic testing.

Original languageEnglish (US)
Pages (from-to)109-114
Number of pages6
JournalClinical Genetics
Issue number1
StatePublished - Jan 1 2016


  • Chromosomal microarray
  • Currarino syndrome
  • Distal 7q deletions
  • MNX1 gene
  • Sequencing
  • Testing algorithm

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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