Literature DB >> 11555456

Fetal akinesia deformation sequence: behavioral development in a case of congenital myopathy.

E J Mulder1, P G Nikkels, G H Visser.   

Abstract

OBJECTIVE: To monitor behavioral development in a fetus affected by the Pena-Shokeir phenotype due to fetal akinesia deformation sequence of myogenic origin.
METHODS: Fetal behavioral development was studied sonographically in a fetus suspected of having fetal akinesia deformation sequence, between 15 and 35 weeks of gestation at 1-4-week intervals.
RESULTS: Fetal body movements were quantitatively and qualitatively abnormal from 28 weeks onwards. Behavioral deterioration coincided with the observation of structural anomalies such as club feet. Fetal heart rate and its variation remained within normal limits and showed normal ultradian cyclicity, but the temporal linkage between body movements and heart rate pattern worsened with advancing gestation. Breathing movements, although present until the end of pregnancy, became increasingly shallow.
CONCLUSION: Our results provide sound evidence that the trajectory of behavioral development with fetal akinesia deformation sequence, which has been hypothesized to occur in man exclusively on the basis of retrospective analyses and animal experiments, does indeed take place.

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Year:  2001        PMID: 11555456     DOI: 10.1046/j.1469-0705.2001.00422.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  4 in total

1.  Prenatal diagnosis of Pena-Shokeir syndrome phenotype by ultrasonography and MR imaging.

Authors:  Efsun Urger Senocak; Kader Karli Oguz; Goknur Haliloglu; Deniz Karcaaltincaba; Deniz Akata; Omer Kandemir
Journal:  Pediatr Radiol       Date:  2009-02-05

2.  The skeleton and musculature on foetal MRI.

Authors:  Ursula Nemec; Stefan F Nemec; Deborah Krakow; Peter C Brugger; Gustavo Malinger; John M Graham; David L Rimoin; Daniela Prayer
Journal:  Insights Imaging       Date:  2011-02-19

Review 3.  Investigation of normal organ development with fetal MRI.

Authors:  Daniela Prayer; Peter C Brugger
Journal:  Eur Radiol       Date:  2007-03-07       Impact factor: 7.034

4.  The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypes.

Authors:  Kit San Yeung; Florrie N Y Yu; Cheuk Wing Fung; Sheila Wong; Hencher H C Lee; Sharon T H Fung; Genevieve P G Fung; Kwok Yin Leung; Wai Hang Chung; Yun Ting Lee; Vivian K S Ng; Mullin H C Yu; Jasmine L F Fung; Mandy H Y Tsang; Kelvin Y K Chan; Sophelia H S Chan; Anita S Y Kan; Brian H Y Chung
Journal:  Mol Genet Genomic Med       Date:  2020-04-30       Impact factor: 2.183

  4 in total

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