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Spina bifida cystica and severe congenital bilateral talipes equinovarus in one twin of a monoamniotic pair: a case report
Authors:Benjamin Momo Kadia  Desmond Aroke  Frank-Leonel Tianyi  Ndemazie Nkafu Bechem  Christian Akem Dimala
Affiliation:1.Foumbot District Hospital,Foumbot,Cameroon;2.Grace Community Health and Development Association,Kumba,Cameroon;3.Health and Human Development (2HD) Research Network,Douala,Cameroon;4.Mbengwi District Hospital,Mbengwi,Cameroon;5.Mayo Darle Sub-Divisional Hospital,Mayo Darle,Cameroon;6.School of Health Sciences,University of Nottingham,Nottingham,UK;7.Faculty of Epidemiology and Population Health,London School of Hygiene and Tropical Medicine,London,UK;8.Department of Orthopaedics,Southend University Hospital,Essex,UK
Abstract:

Background

Spina bifida and congenital talipes equinovarus (CTEV) are common congenital malformations which may occur together and increase morbidity. Monozygous twins are particularly at risk of these malformations and discordance in one type of malformation is typical. The occurrence of both spina bifida and CTEV in one twin of a monozygotic pair is rare.

Case presentation

A 22 year-old Cameroonian primigravida at 36 weeks of a twin gestation was received in our district hospital at the expulsive phase of labour on a background of sub-optimal antenatal care. A caesarean section indicated for cephalo-pelvic disproportion was performed and life monoamniotic male twins were extracted. The first twin was normal. The second twin had spina bifida cystica and severe bilateral CTEV. Routine postnatal care was ensured and at day 2 of life, the affected twin was evacuated to a tertiary hospital for proper management. He was later on reported dead from complications of hydrocephalus.

Conclusions

Spina bifida cystica with severe bilateral CTEV in one twin of a monoamniotic pair illustrates the complexity in the interplay of causal factors of these malformations even among monozygotic twins who are assumed to share similar genetic and environmental features. The occurrence and poor outcome of the malformations was probably potentiated by poor antenatal care. With postnatal diagnoses, a better outcome was difficult to secure even with prompt referral. Early prenatal diagnoses and appropriate counseling of parents are cardinal.
Keywords:
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