Pena-Shokeir syndrome: current management strategies and palliative care
Sumaiya Adam,1 Melantha Coetzee,2 Engela Magdalena Honey3 1Department of Obstetrics and Gynaecology, Steve Biko Academic Hospital, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa; 2Division of Neonatology, Department of Pediatrics and Child Health, Steve Biko Academic Hosp...
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doaj-490af91821264ad59ab61d7af403ff082020-11-25T00:55:09ZengDove Medical PressThe Application of Clinical Genetics1178-704X2018-10-01Volume 1111112041765Pena-Shokeir syndrome: current management strategies and palliative careAdam SCoetzee MHoney EMSumaiya Adam,1 Melantha Coetzee,2 Engela Magdalena Honey3 1Department of Obstetrics and Gynaecology, Steve Biko Academic Hospital, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa; 2Division of Neonatology, Department of Pediatrics and Child Health, Steve Biko Academic Hospital, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa; 3Department of Biochemistry, Genetics and Microbiology, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa Abstract: Pena–Shokeir syndrome (PSS) type 1, also known as fetal akinesia deformation sequence, is a rare genetic syndrome that almost always results in intrauterine or early neonatal death. It is characterized by markedly decreased fetal movements, intrauterine growth restriction, joint contractures, short umbilical cord, and features of pulmonary hypoplasia. Antenatal ­diagnosis can be difficult. Ultrasound features are varied and may overlap with those of ­Trisomy 18. The poor prognosis of PSS is due to pulmonary hypoplasia, which is an important feature that distinguishes PSS from arthrogryposis multiplex congenital without pulmonary hypoplasia, which has a better prognosis. If diagnosed in the antenatal period, a late termination of pregnancy can be considered following ethical discussion (if the law allows). In most cases, a diagnosis is only made in the neonatal period. Parents of a baby affected with PSS require detailed counseling that includes information on the imprecise recurrence risks and a plan for subsequent pregnancies. Keywords: fetal akinesia deformation sequence, ultrasound, comfort carehttps://www.dovepress.com/pena-shokeir-syndrome-current-management-strategies-and-palliative-car-peer-reviewed-article-TACGfetal akinesia deformation sequenceultrasoundcomfort care |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Adam S Coetzee M Honey EM |
spellingShingle |
Adam S Coetzee M Honey EM Pena-Shokeir syndrome: current management strategies and palliative care The Application of Clinical Genetics fetal akinesia deformation sequence ultrasound comfort care |
author_facet |
Adam S Coetzee M Honey EM |
author_sort |
Adam S |
title |
Pena-Shokeir syndrome: current management strategies and palliative care |
title_short |
Pena-Shokeir syndrome: current management strategies and palliative care |
title_full |
Pena-Shokeir syndrome: current management strategies and palliative care |
title_fullStr |
Pena-Shokeir syndrome: current management strategies and palliative care |
title_full_unstemmed |
Pena-Shokeir syndrome: current management strategies and palliative care |
title_sort |
pena-shokeir syndrome: current management strategies and palliative care |
publisher |
Dove Medical Press |
series |
The Application of Clinical Genetics |
issn |
1178-704X |
publishDate |
2018-10-01 |
description |
Sumaiya Adam,1 Melantha Coetzee,2 Engela Magdalena Honey3 1Department of Obstetrics and Gynaecology, Steve Biko Academic Hospital, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa; 2Division of Neonatology, Department of Pediatrics and Child Health, Steve Biko Academic Hospital, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa; 3Department of Biochemistry, Genetics and Microbiology, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa Abstract: Pena–Shokeir syndrome (PSS) type 1, also known as fetal akinesia deformation sequence, is a rare genetic syndrome that almost always results in intrauterine or early neonatal death. It is characterized by markedly decreased fetal movements, intrauterine growth restriction, joint contractures, short umbilical cord, and features of pulmonary hypoplasia. Antenatal ­diagnosis can be difficult. Ultrasound features are varied and may overlap with those of ­Trisomy 18. The poor prognosis of PSS is due to pulmonary hypoplasia, which is an important feature that distinguishes PSS from arthrogryposis multiplex congenital without pulmonary hypoplasia, which has a better prognosis. If diagnosed in the antenatal period, a late termination of pregnancy can be considered following ethical discussion (if the law allows). In most cases, a diagnosis is only made in the neonatal period. Parents of a baby affected with PSS require detailed counseling that includes information on the imprecise recurrence risks and a plan for subsequent pregnancies. Keywords: fetal akinesia deformation sequence, ultrasound, comfort care |
topic |
fetal akinesia deformation sequence ultrasound comfort care |
url |
https://www.dovepress.com/pena-shokeir-syndrome-current-management-strategies-and-palliative-car-peer-reviewed-article-TACG |
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