Rare case of congenital anomaly in two different gestational ages: a case series

Authors

  • Lopamudra B. John Department of Obstetrics & Gynecology, Mahatma Gandhi Medical College and Research Institute, Pilliarkuppam, Pondicherry-607402, India
  • Sendhil Coumary A Department of Obstetrics & Gynecology, Mahatma Gandhi Medical College and Research Institute, Pilliarkuppam, Pondicherry-607402, India
  • Seetesh Ghose Department of Obstetrics & Gynecology, Mahatma Gandhi Medical College and Research Institute, Pilliarkuppam, Pondicherry-607402, India

Keywords:

Acrania, Anencephaly

Abstract

Acrania is a rare congenital anomaly involving faulty development of membranous flat bones of neurocalvarium. Commonest differential diagnosis is anencephaly. The first case was diagnosed in a second gravida at 13 weeks and terminated by vaginal misoprostol instillation. The second case was diagnosed only by scan at 32 weeks in an unbooked second gravida with previous LSCS. She underwent emergency LSCS for failed induction and a fresh stillborn baby of 1.9 kg was born.

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Published

2016-12-09

How to Cite

John, L. B., Coumary A, S., & Ghose, S. (2016). Rare case of congenital anomaly in two different gestational ages: a case series. International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 2(2), 240–241. Retrieved from https://www.ijrcog.org/index.php/ijrcog/article/view/222

Issue

Section

Case Reports