HEMIHYDRANENCEPHALY; A CASE REPORT

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BALPANDE D.N.; PATHAK CH.SH.; AGRAWAL A.; SINGH B.R.

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Journal Paper

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Journal: Iranian Journal of Pediatrics Year:2009 | Volume:19 | Issue:2 Page(s): 180-184

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Title

HEMIHYDRANENCEPHALY; A CASE REPORT

Author(s)

BALPANDE D.N. | PATHAK CH.SH. | AGRAWAL A. | SINGH B.R. | Issue Writer Certificate

Keywords

HEMIHYDRANENCEPHALY

BRAIN

CONGENITAL ANOMALIES

CAROTID ARTERY

APLASIA

Abstract

Background: HEMIHYDRANENCEPHALY is a rare disorder of the BRAIN characterized by complete or almost complete unilateral absence of cerebral cortex with preservation of meninges, basal ganglia, pons, medulla, cerebellum, and falx.Case Presentation: Thirteen year-old male child presented with left sided upper and lower limb weakness with facial asymmetry since the age of six months. His magnetic resonance imaging (MRI) scans demonstrated a nearly complete absence of the right cerebral hemisphere including basal ganglion, which was replaced by cerebrospinal fluid with a small residual rim of the occipital cortex. The imaging features were suggestive of right-sided HEMIHYDRANENCEPHALY.Conclusion: Patients with HEMIHYDRANENCEPHALY provide an experiment of nature with potential implications for normal cognitive development and illustrate how much there is still to be learned about human development.

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APA: Copy

BALPANDE, D.N., PATHAK, CH.SH., AGRAWAL, A., & SINGH, B.R.. (2009). HEMIHYDRANENCEPHALY; A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS, 19(2), 180-184. SID. https://sid.ir/paper/549927/en

Vancouver: Copy

BALPANDE D.N., PATHAK CH.SH., AGRAWAL A., SINGH B.R.. HEMIHYDRANENCEPHALY; A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2009;19(2):180-184. Available from: https://sid.ir/paper/549927/en

IEEE: Copy

D.N. BALPANDE, CH.SH. PATHAK, A. AGRAWAL, and B.R. SINGH, “HEMIHYDRANENCEPHALY; A CASE REPORT,” IRANIAN JOURNAL OF PEDIATRICS, vol. 19, no. 2, pp. 180–184, 2009, [Online]. Available: https://sid.ir/paper/549927/en

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