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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Novel MNX1 mutations and genotype–phenotype analysis of patients with Currarino syndrome

Fig. 2

Pedigrees of the 9 families detected to carry pathogenic MNX1 mutations in this study. Individuals with CS are indicated by solid squares (male) or solid circles (female). Affected individuals with MNX1 mutations who have changes apparent only on an MRI are indicated by a black diagonal stripe. Asymptomatic individuals who have MNX1 mutations are indicated by a gray diagonal stripe

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