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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Main Authors: Adam S, Coetzee M, Honey EM
Format: Article
Language:English
Published: Dove Medical Press 2018-10-01
Series:The Application of Clinical Genetics
Subjects:
Online Access:https://www.dovepress.com/pena-shokeir-syndrome-current-management-strategies-and-palliative-car-peer-reviewed-article-TACG
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spelling 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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