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Case Studies | Pediatrics | India | Volume 4 Issue 1, January 2015
A Rare Case of Acrocallosal Syndrome in a Neonate - A Case Report
S. Lakshmi [11] | G. Fatima Shirly Anitha [2] | S. Vinoth [3]
Abstract: Acrocallosal syndrome is characterised by classical craniofacial and digital malformations with partial or complete agenesis of corpus callosum. This is considered as a rare disorder and is included in the Rare Diseases list of the National Institute of Health (NIH), which means there are fewer than 200, 000 cases). Here we report one such rare case of acrocallosal syndrome diagnosed in a neonate with characteristic clinical features and neuroimaging findings of partial agenesis of corpus callosum and arachnoid cyst in posterior fossa.
Keywords: Acrocallosal syndrome, Corpus callosum agenesis, Posterior fossa cyst
Edition: Volume 4 Issue 1, January 2015,
Pages: 979 - 981
Similar Articles with Keyword 'syndrome'
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Case Studies, Pediatrics, India, Volume 11 Issue 6, June 2022
Pages: 847 - 850A Case Report on Systemic Lupus Erythematosis, Lupus Nephritis, Acute Pancreatitis, Posterior Reversible Encephalopathy Syndrome (PRES), Macrophage Activating Syndrome (MAS)
S. Mohamed Ashik Ali | P. Muhammed Nishad | A. Priya [3] | K. Arun Chander
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Case Studies, Pediatrics, India, Volume 11 Issue 6, June 2022
Pages: 1559 - 1560Rare Case Report on Incontinentia Pigmenti
Dr. Tinkal Patel | Dr. Devavrat Bhide | Dr. Panna Patel | Dr. Apoorva Shah