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|Case Report|| |
A newborn with a missing cerebrum
Anne Weissenstein, Gloria Villalon, Elisabeth Luchter, Stefan Bittmann.
Hydranencephaly is an extremely rare anomaly of cerebral structures that occurs in-utero. Cerebral hemispheres are destroyed with transformation into a membranous sac with cerebrospinal fluid and parts of cortex and white matter. The disorder has an incidence of 0.2% in children. Clinical symptoms in neonates are seizures, respiratory failure, flaccidity or decerebrate posturing. Complete absence of the cerebral hemispheres and falx is present. We present a case of a male newborn with hydranencephaly. A possible correlation with in utero exposure to vasoactive drugs will be discussed.
Child, drug abuse, hydranencephaly
|1. Kurtz AB, Johnson PT. Diagnosis please. Case 7: Hydranencephaly. Radiology 1999;210:419-22. [DOI via Crossref] [Pubmed] |
|2. Malik AM, Ahmad M, Khan A, Ullah E. Hydranencephaly: a rare cause of delayed developmental milestones. BMJ Case Rep 2013;2013:pii: bcr2013009589.|
|3. Pavone P, Nigro F, Falsaperla R, Greco F, Ruggieri M, Rizzo R, et al. Hemihydranencephaly: living with half brain dysfunction. Ital J Pediatr 2013;39:3. [DOI via Crossref] [Pubmed] [PMC Free Fulltext] |
|4. Ghosh PS, Reid JR, Patno D, Friedman NR. Fetal magnetic resonance imaging in hydranencephaly. J Paediatr Child Health 2013;49:335-6. [DOI via Crossref] [Pubmed] |
|5. Cecchetto G, Milanese L, Giordano R, Viero A, Suma V, Manara R. Looking at the missing brain: hydranencephaly case series and literature review. Pediatr Neurol 2013;48:152-8. [DOI via Crossref] [Pubmed] |