Literature DB >> 3077584

Lower limb movements and urologic function in fetuses with neural tube and other central nervous system defects.

S L Warsof1, J S Abramowicz, S K Sayegh, D L Levy.   

Abstract

Lower limb movements and urologic systems were evaluated by prenatal ultrasound in 120 fetuses with either neural tube defects or intracranial anomalies. Despite anticipated major lower extremity and bladder dysfunction, lower limb movements were seen in 100% of the fetuses with anencephaly and encephaloceles, 93% with isolated spina bifida, 60% with complex spina bifida and 90% with abnormal intracranial findings. In all the cases except those with cloacal exstrophy, fetal bladder and collecting systems appeared normal. Therefore, fetal lower limb movements and urinary tract integrity appear to have no diagnostic or prognostic value in fetuses with neural tube defects or other central nervous system anomalies. These diagnoses can only be made by direct ultrasound observation of the lesion itself.

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Year:  1988        PMID: 3077584     DOI: 10.1159/000263344

Source DB:  PubMed          Journal:  Fetal Ther        ISSN: 0257-2788


  4 in total

1.  Approximate entropy values demonstrate impaired neuromotor control of spontaneous leg activity in infants with myelomeningocele.

Authors:  Beth A Smith; Caroline Teulier; Jennifer Sansom; Nicholas Stergiou; Beverly D Ulrich
Journal:  Pediatr Phys Ther       Date:  2011       Impact factor: 3.049

2.  Stepping responses of infants with myelomeningocele when supported on a motorized treadmill.

Authors:  Caroline Teulier; Beth A Smith; Masayoshi Kubo; Chia-Lin Chang; Victoria Moerchen; Karin Murazko; Beverly D Ulrich
Journal:  Phys Ther       Date:  2008-12-04

3.  Muscle activation patterns in infants with myelomeningocele stepping on a treadmill.

Authors:  Jennifer K Sansom; Caroline Teulier; Beth A Smith; Victoria Moerchen; Karin Muraszko; Beverly D Ulrich
Journal:  Pediatr Phys Ther       Date:  2013       Impact factor: 3.049

4.  Cell necrosis, intrinsic apoptosis and senescence contribute to the progression of exencephaly to anencephaly in a mice model of congenital chranioschisis.

Authors:  Marc Oria; Soner Duru; Rebeca L Figueira; Federico Scorletti; Lucas E Turner; Irati Fernandez-Alonso; Alejandra Fernandez-Martin; Mario Marotta; Lourenco Sbragia; Aimen F Shaaban; Jose L Peiro
Journal:  Cell Death Dis       Date:  2019-09-26       Impact factor: 8.469

  4 in total

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