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. 2017 Jan 23:26:30.
doi: 10.11604/pamj.2017.26.30.11525. eCollection 2017.

Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter

[Article in French]
Affiliations

Schinzel-Giedion syndrome: a case with sacrococcygeal teratoma and cor-triatriatum dexter

[Article in French]
Lofty-John Anyanwu et al. Pan Afr Med J. .

Abstract

Schinzel-Giedion syndrome which is associated with midfacial hypoplasia and coarse dysmorphic features is a multiple congenital malformation syndrome. It is believed that risk of malignancy may be a component of the anomaly. We report herein a case of a 16 months old boy with SGS associated with sacrococcygeal teratoma and cor-triatriatum dexter. Histopathology report of the excised sacrococcygeal mass showed no malignant foci. He was however lost to follow up in the second week post-operation.

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Conflict of interest statement

The authors declare no competing interest.

Figures

Figure 1
Figure 1
Frontal view (A) and right lateral view (B) of a child with Schinzel-Giedion syndrome. Note the tall fore head, hypertelorism and microtic protruded ear lobes
Figure 2
Figure 2
Sacrococcygeal mass in the same patient
Figure 3
Figure 3
(A) subcostal view and (B) apical four chamber view of transthoracic echocardiography of the patient, showing a thick band of echogenic tissue dividing the right atrium into 2 unequal halves

References

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