Neuropediatrics 1997; 28(2): 116-119
DOI: 10.1055/s-2007-973683
Original articles

© Hippokrates Verlag GmbH Stuttgart

Fetal Akinesia Sequence Caused by Nemaline Myopathy

M. Lammens1 , 2 , Ph. Moerman3 , J. P. Fryns4 , F. Lemmens5 , G. M. van de Kamp6 , N. Goemans7 , R. Dom2
  • 1Stichting PAMM, Catharinaziekenhuis, Eindhoven, The Netherlands;
  • 2Departments of Neuropathology, University Hospital Gasthuisberg, Leuven, Belgium
  • 3Departments of Pathology I University Hospital Gasthuisberg, Leuven, Belgium
  • 4Center of Human Genetics, University Hospital Gasthuisberg, Leuven, Belgium
  • 5Department of Pediatrics, St-Jansziekenhuis, Genk, Belgium;
  • 6Neonatal Intensive Care Unit, St-Josephziekenhuis, Veldhoven, The Netherlands
  • 7Departments of Pediatrics, University Hospital Gasthuisberg, Leuven, Belgium
Further Information

Publication History

Publication Date:
13 March 2007 (online)

Abstract

Nine patients with the characteristic signs of fetal akinesia sequence (polyhydramnion, multiple joint contractures and lung hypoplasia) are described. In 8 of the 9 patients nemaline myopathy could be demonstrated with histology. The ninth patient presented the same phenotype as his 4 affected siblings in whom the nemaline myopathy could be histologically proven. Seven of the patients belonged to 2 families; the other 2 patients were isolated cases. In one fetal case nemaline myopathy was documented at week 22 of gestation. These observations demonstrate that nemaline myopathy can cause the fetal akinesia sequence, with onset of first symptoms as early as the beginning of the second trimester of pregnancy.

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