We report on 8 patients from two families with Alpers syndrome. The onset in one family was prenatal and in the 4 patients who were examined, severe microcephaly, intrauterine growth retardation, and typical manifestations of fetal akinesia, including retrog nathia, joint limitations, and chest defo
✦ LIBER ✦
Progressive infantile poliodystrophy (alpers' disease) and disorders of pyruvate metabolism
✍ Scribed by Prick, M.; Gabreëls, F.J.M.; Trijbels, F.; Renier, W.; Janssen, A.; Jaspar, H.; Slooff, J.L.
- Book ID
- 122070707
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 146 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0303-8467
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