Recurrent Congenital Diaphragmatic Hernia in Ehlers-Danlos Syndrome
β Scribed by I. Chun Lin; Sheung Fat Ko; Chie Song Shieh; Chien Fu Huang; Shao Ju Chien; Chi Di Liang
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 109 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1432-086X
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## Abstract Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome involving the Wilms tumor 1 gene (__WT1__), the paired box gene 6 (__PAX6__), and possibly other genes on chromosome 11p13. __WT1__ is required for normal format
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