The sequence of acrania–exencephaly–anencephaly (AEAS)- An infrequent case report

Author:

Shenoy Heera Trivikrama1ORCID,Kunju Najah Ismail2,Khan Naseemabeevi Ahmed3,Puthanayil Sudhya P3,Ambujakshan Sangeetha Ambujakshan3

Affiliation:

1. Malabar Medical College Hospital and Research Center, Kozhikode, Kerala, India

2. KMCT Medical College, Manassery, Kerala, India

3. KMCT Medical College, Kozhikode,

Abstract

Acrania–exencephaly–anencephaly sequence has an incidence of 3.6–5.4 for 10,000 live births and has been reported in literature. Exencephaly, described here is a defect of the neural tube which occurs due to the absence of closure of the neural fold. The main diagnostic ultrasound features include that are characterized by acrania, decreased size of cranial pole in comparison with the chest, irregular cranial surface, with increased amniotic fluid echogenicity due to the damaged brain tissue. Associated with amniotic band syndrome, Pentalogy of Cantrell, limb anomalies and ventral body wall defects. It is incompatible with life. Conducting programs training the budding neuro-sonographers about the knowledge in detection, diagnosis of NTD according to the Carnegie Classification is crucial to look forward in pathogenesis and application in the clinical scenario.

Publisher

IP Innovative Publication Pvt Ltd

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