Anencephaly: a case report on the rare neural tube defect

Anencephaly is a severe, lethal, neural tube defect characterized by the partial or total absence of the brain and calvarium, with a 100% mortality rate either in utero or shortly after birth. It occurs when anterior neuropore fails to close between 23-26 days post-conception, affecting approximately 1 per 1,000 births and is associated with genetic and environmental risk factors such as maternal diabetes, obesity, toxin exposure, and folate deficiency. The condition can be diagnosed early in pregnancy, usually between the 11th and 14th weeks of pregnancy, by USG identifying the lack of cranial ossification and failure to measure the biparietal diameter and also detection through maternal serum alpha-fetoprotein levels. Early diagnosis is essential for effective management and counselling, particularly because of the high likelihood of pregnancy termination due to the fatal prognosis.

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Publication Details

Journal
International Journal of Reproduction Contraception Obstetrics and Gynecology
Published
2024-10-28
DOI
https://doi.org/10.18203/2320-1770.ijrcog20243209
Primary Topic
Fetal and Pediatric Neurological Disorders
Type
article
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article

Anencephaly: a case report on the rare neural tube defect

Subban Ravi, Usha Devi Gopalan, Florence Nightingle Sagar
International Journal of Reproduction Contraception Obstetrics and Gynecology
Fetal and Pediatric Neurological Disorders
article

Anencephaly: a case report on the rare neural tube defect

Subban Ravi, Usha Devi Gopalan, Florence Nightingle Sagar
article en

Abstract

Anencephaly is a severe, lethal, neural tube defect characterized by the partial or total absence of the brain and calvarium, with a 100% mortality rate either in utero or shortly after birth. It occurs when anterior neuropore fails to close between 23-26 days post-conception, affecting approximately 1 per 1,000 births and is associated with genetic and environmental risk factors such as maternal diabetes, obesity, toxin exposure, and folate deficiency. The condition can be diagnosed early in pregnancy, usually between the 11th and 14th weeks of pregnancy, by USG identifying the lack of cranial ossification and failure to measure the biparietal diameter and also detection through maternal serum alpha-fetoprotein levels. Early diagnosis is essential for effective management and counselling, particularly because of the high likelihood of pregnancy termination due to the fatal prognosis.

International Journal of Reproduction Contraception Obstetrics and GynecologyVol. 13(11)
Shri Sathya Sai Medical College and Research Institute (IN)
Good health and well-being
Openalex Percentile: Top 70%
Fetal and Pediatric Neurological Disorders
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