Cerebrovascular complications in Ehlers-Danlos syndrome type IV
β Scribed by Kathryn N. North; David A. H. Whiteman; Melanie G. Pepin; Dr Peter H. Byers
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 536 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0364-5134
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Ehlers-Danlos syndrome type VIII (EDS VIII) is a rare disorder of unknown cause inherited in an autoso-ma1 dominant mode. Specific alterations in the synthesis or secretion of collagens I and 111, or ultrastructural abnormalities of skin fibroblasts and extracellular matrix, have not been demonstrat
## Abstract ## Objective EhlersβDanlos syndrome (EDS) is a clinically and genetically heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Muscle involvement is plausible based on recently discovered inter
of motor unit action potential-like discharges (Fig. ); they disappeared during sleep. With the needle in the masseter, a spatula test 1 was performed. It was positive, and could be documented by EMG monitoring. This case suggests that NNT should be kept in mind and always be considered in neonates