Neuropediatrics 1986; 17(3): 132-136
DOI: 10.1055/s-2008-1052514
© Georg Thieme Verlag KG Stuttgart · New York

Hypomyelination Neuropathy in a Female Newborn Presenting as Arthrogryposis Multiplex Congenita

R. J. Seitz1 , W.  Wechsler1 , D. S. Mosny2 , H. G. Lenard3
  • 1Department of Neuropathology, University of Düsseldorf, Moorenstr. 5, D-4000 Düsseldorf 1, FRG
  • 2Department of Pathology, University of Düsseldorf, Moorenstr. 5, D-4000 Düsseldorf 1, FRG
  • 3Department of Pediatrics, University of Düsseldorf, Moorenstr. 5, D-4000 Düsseldorf 1, FRG
Further Information

Publication History

Publication Date:
16 May 2008 (online)

Abstract

A female newborn delivered at 32 weeks of gestation presented with multiple joint contractures consistent with arthrogryposis multiplex congenita (AMC). The girl died after a four days course of severe respiratory distress. Autopsy revealed slightly hypoplastic and immature lungs with acute necrotizing bronchopneumonia, and marked consecutive hypoxic brain lesions with severe periventricular haemorrhages. The peripheral nerves including the cranial and spinal nerve roots showed a hypomyelination radiculoneuropathy with well preserved axons and a normal content of Schwann cells. In the skeletal muscles of the arms and legs some fascicles of the extensors were replaced by lipomatous tissue. Since myelination of the white matter in the central nervous system was adequate to the age, this case represents an exclusive maturation disorder of the peripheral myelin sheaths that may be considered causal for AMC.