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Journal of Obstetrics and Gynaecology Volume 33, 2013 - Issue 3
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GYNAECOLOGY CASE REPORTS

Anomalous ovarian morphology in a patient with craniofrontonasal syndrome

S. RundleDepartment of Obstetrics and Gynaecology, North Devon District Hospital, BarnstapleCorrespondence[email protected]
,
B. CastleDepartment of Clinical Genetics, Royal Devon and Exeter Hospital, Exeter, UK
&
S. D. EckfordDepartment of Obstetrics and Gynaecology, North Devon District Hospital, Barnstaple
Page 316 | Published online: 03 Apr 2013

References

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  • Slover R, Sujansky E. 1979. Frontonasal dysplasia with coronal craniosynostosis in three sibs. Birth Defects Original Article Series 15:75–83.
  • Twigg SRF, Kan R, Babbs C . 2004. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. Proceedings of the National Academy of Science of the USA 8:8652–8657.
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  • Wieacker P, Wieland I. 2005. Clinical and genetic aspects of craniofrontonasal syndrome: Towards resolving a genetic paradox. Molecular Genetics and Metabolism 86:110–116.

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