A novel type of familial proximal axonal dystrophy: Three cases and a review of the axonal dystrophies

• Type: Another Publication in an International Scientific Journal
• Date: 2012

Authors

Carpenter, S (Author) Other; Henrique Soares (Author) FMUP; Brandao, O (Author) Other; Moura, CS (Author) Other; Castro, L (Author) Other; Rodrigues, E (Author) Other; Cunha, AL (Author) Other; Bartosch, C (Author) Other

Journal

Title: European Journal of Paediatric Neurology

Vol. 16

Pages: 292-300

ISSN: 1090-3798

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 2 Citations

Scopus - 2 Citations

Other information

Authenticus ID: P-002-AHW

DOI: 10.1016/j.ejpn.2011.08.010

Abstract (EN): Three related infants of Roma ancestry, two of them siblings, showed hypotonia, predominantly axial, from birth, difficulty swallowing, myoclonic seizures, and respiratory difficulty. Dysmorphic features, principally micrognathia were present. EEGs showed focal epileptiform abnormalities. All three died in their 5th month from respiratory insufficiency complicated by pneumonia. Autopsy showed small brains without malformation. Microscopy revealed numerous axonal spheroids involving particularly the brain stem and spinal cord, with especial prominence in the middle cerebellar peduncle, the anterior part of the thalamic reticular nuclei, and the anterior horns and columns of the spinal cord. Spheroids that appeared to be on axons of lower motor neurons were especially large. No spheroids were seen in peripheral nerves; electron microscopy did not show spheroids in skin. By electron microscopy spheroids contained neurofilaments, sparse mitochondria, and electron dense granules. The material did not allow identification of microtubules. Closely packed vesicles excluded neurofilamanets from the center of many spheroids, especially in the middle cerebellar peduncle. Sprouting of axons from the surface of many spheroids was seen. This disease is distinct from the well described type of infantile neuroaxonal dystrophy (Seitelberger's disease) in view of the distribution of spheroids, presence of spheroids on proximal rather than distal parts of axons, sparing of the peripheral nerves, lack of staining for synuclein, presence of sprouting, and lack of membranous profiles in the spheroids. A review of reported types of axonal dystrophy has not shown identical cases.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9