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Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects

Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformational changes resulting from decreased or absent fetal movement, and include arthrogryposis, and craniofacial and central nervous system anomalies. We report an autopsy case of a 36-6/7week female neo...

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Autores principales: Kapp, Meghan Elizabeth, Lyle, Pamela, Nickols, Hilary Highfield
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital Universitário da Universidade de São Paulo 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432359/
https://www.ncbi.nlm.nih.gov/pubmed/34540727
http://dx.doi.org/10.4322/acr.2021.323
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author Kapp, Meghan Elizabeth
Lyle, Pamela
Nickols, Hilary Highfield
author_facet Kapp, Meghan Elizabeth
Lyle, Pamela
Nickols, Hilary Highfield
author_sort Kapp, Meghan Elizabeth
collection PubMed
description Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformational changes resulting from decreased or absent fetal movement, and include arthrogryposis, and craniofacial and central nervous system anomalies. We report an autopsy case of a 36-6/7week female neonate with a normal female karyotype and chromosome microarray demonstrating findings consistent with FADS. We provide a detailed examination of the severe and complex central nervous system abnormalities, including marked pontocerebellar hypoplasia and cortical and cerebellar migration and gyration defects. This case represents a rare detailed examination of the central nervous system of a patient with FADS.
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spelling pubmed-84323592021-09-17 Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects Kapp, Meghan Elizabeth Lyle, Pamela Nickols, Hilary Highfield Autops Case Rep Autopsy Case Report Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformational changes resulting from decreased or absent fetal movement, and include arthrogryposis, and craniofacial and central nervous system anomalies. We report an autopsy case of a 36-6/7week female neonate with a normal female karyotype and chromosome microarray demonstrating findings consistent with FADS. We provide a detailed examination of the severe and complex central nervous system abnormalities, including marked pontocerebellar hypoplasia and cortical and cerebellar migration and gyration defects. This case represents a rare detailed examination of the central nervous system of a patient with FADS. Hospital Universitário da Universidade de São Paulo 2021-09-03 /pmc/articles/PMC8432359/ /pubmed/34540727 http://dx.doi.org/10.4322/acr.2021.323 Text en Copyright © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Autopsy Case Report
Kapp, Meghan Elizabeth
Lyle, Pamela
Nickols, Hilary Highfield
Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title_full Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title_fullStr Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title_full_unstemmed Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title_short Fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
title_sort fetal akinesia deformation sequence with pontocerebellar hypoplasia, and migration and gyration defects
topic Autopsy Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432359/
https://www.ncbi.nlm.nih.gov/pubmed/34540727
http://dx.doi.org/10.4322/acr.2021.323
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