Middle interhemispheric variant of holoprosencephaly – Presenting as non-visualized cavum septum pellucidum and an interhemispheric cyst in A 19-weeks fetus

Akhila Vasudevava, Shalini S. Nayak, Rajagopal Kadavavigere, Katta M. Girisha, Jyothi Shetty

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Middle Interhemispheric variant (MIH) is a rare subtype of holoprosencephaly (HPE), also known as syntelencephaly. We present a case of MIH, which was diagnosed as an interhemispheric cyst on antenatal sonography at 19 weeks, but later diagnosed as MIH variant of holoprosencephaly after a postabortal MRI and perinatal autopsy.

Original languageEnglish
Pages (from-to)QD11-QD13
JournalJournal of Clinical and Diagnostic Research
Volume9
Issue number9
DOIs
Publication statusPublished - 01-09-2015

Fingerprint

Septum Pellucidum
Holoprosencephaly
Ultrasonography
Magnetic resonance imaging
Cysts
Fetus
Autopsy

All Science Journal Classification (ASJC) codes

  • Medicine(all)
  • Clinical Biochemistry

Cite this

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Middle interhemispheric variant of holoprosencephaly – Presenting as non-visualized cavum septum pellucidum and an interhemispheric cyst in A 19-weeks fetus. / Vasudevava, Akhila; Nayak, Shalini S.; Kadavavigere, Rajagopal; Girisha, Katta M.; Shetty, Jyothi.

In: Journal of Clinical and Diagnostic Research, Vol. 9, No. 9, 01.09.2015, p. QD11-QD13.

Research output: Contribution to journalArticle

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AU - Nayak, Shalini S.

AU - Kadavavigere, Rajagopal

AU - Girisha, Katta M.

AU - Shetty, Jyothi

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