Literature DB >> 3561701

The pathogenesis of fetal hypokinesia. A neurological study of 75 cases of congenital contractures with emphasis on cerebral lesions.

G Hageman, J Willemse, B A van Ketel, A F Verdonck.   

Abstract

A comprehensive prospective clinical study is presented of 75 cases of fetal hypokinesia and congenital contractures of various causes, with neuropathological investigation in 23 cases. With the data of medical history, neurological examination, laboratory tests and neuropathology an exact or probable nosological or syndromal diagnosis could be made in 61 cases. These cases were categorized by localisation of causal pathology in the subsequent levels of the developing motor system. In 14 of 61 cases developmental brain disorders (f.i. hydrocephalus, hydranencephaly, microcephaly) were the cause of fetal hypokinesia, often with perinatal death, whereas in 7 cases both cerebral and/or spinal cord lesions were found. Besides cerebral involvement was frequently present in cases with congenital contractures of other origin, concomitant or due to perinatal complications. In a large number of cases clinical evidence of spinal cord lesions, especially anterior horn cell degeneration was present. Myopathic disorders occurred in only four cases, whereas congenital myasthenia and congenital neuropathy were present in one case each. In cases without muscle weakness miscellaneous disorders including congenital skin anomalies and probably primary connective tissue disorders were encountered. The etiologic role of intrauterine viral infection is discussed.

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Year:  1987        PMID: 3561701     DOI: 10.1055/s-2008-1052430

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  7 in total

1.  Familial fetal akinesia deformation sequence with a skeletal muscle maturation defect.

Authors:  K Vuopala; F Pedrosa-Domellöf; R Herva; J Leisti; L E Thornell
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

2.  Lethal congenital contracture syndrome: further delineation and genetic aspects.

Authors:  K Vuopala; R Herva
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

3.  Inherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasia.

Authors:  John C Fyfe; Raba' A Al-Tamimi; Rudy J Castellani; Diana Rosenstein; Daniel Goldowitz; Paula S Henthorn
Journal:  J Comp Neurol       Date:  2010-09-15       Impact factor: 3.215

4.  Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs.

Authors:  G Hageman; V T Ramaekers; B G Hilhorst; A R Rozeboom
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-04       Impact factor: 10.154

5.  Hypoplasia of posterior spinal roots and dorsal spinal tracts with arthrogryposis multiplex congenita.

Authors:  H Vogel; D Halpert; D S Horoupian
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

6.  International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita.

Authors:  Noémi Dahan-Oliel; Sarah Cachecho; Douglas Barnes; Tanya Bedard; Ann M Davison; Klaus Dieterich; Maureen Donohoe; Alicja Fąfara; Reggie Hamdy; Helgi T Hjartarson; Naimisha S Hoffman; Eva Kimber; Igor Komolkin; Ruth Lester; Eva Pontén; Harold J P van Bosse; Judith G Hall
Journal:  Am J Med Genet C Semin Med Genet       Date:  2019-07-07       Impact factor: 3.908

7.  The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.

Authors:  Annapurna Poduri; Vida Chitsazzadeh; Stefano D'Arrigo; Ermellina Fedrizzi; Chiara Pantaleoni; Daria Riva; Claudia Busse; Helmut Küster; Adre Duplessis; John Gaitanis; Mustafa Sahin; Cheryl Garganta; Meral Topcu; Kira A Dies; Brenda J Barry; Jennifer Partlow; A James Barkovich; Christopher A Walsh; Bernard S Chang
Journal:  Brain Dev       Date:  2009-09-13       Impact factor: 1.961

  7 in total

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