## Marfan syndrome (MFS) is an autosomal dominant trait due to mutations in the fibrillin gene (FBN1). The MFS expressivity is variable, and its diagnosis relies completely on clinical criteria. Atypical cases and Marfan-like (marfanoid) clinical presentations are commonly found. The metacarpophal
Hiatus/paraesophageal hernias in neonatal Marfan syndrome
β Scribed by Parida, Saroj K.; Kriss, Vesna Martich; Hall, Bryan D.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 13 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19971017)72:2<156::aid-ajmg6>3.0.co;2-t
No coin nor oath required. For personal study only.
β¦ Synopsis
We report on an infant with neonatal Marfan syndrome (NMS) and hiatus/ paraesophageal hernia who presented to a university hospital with an unusual early complication of this connective tissue disorder. An abnormal course of the nasogastric tube was noted on the first day of life by a radiograph of the chest and abdomen performed for bloody gastric drainage. The question of esophageal perforation was raised. Subsequent contrast study demonstrated a large hiatus/paraesophageal hernia with pronounced gastroesophageal reflux (GER). A part of the hernia was positioned posterior and to the right of the gastroesophageal junction (GEJ), presumably the location of the nasogastric tube as noted on the initial films. Although characterized by cardiac/aortic abnormalities, NMS can be a difficult diagnosis and should be considered in any infant with hiatus/ paraesophageal hernia with or without GER.
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**Her vacation timeshare has a "tiny" problem. There's a grumpy naked man in her bed.** **Janae Williams** has taken a sabbatical to finish her first stand-alone research book. All she needs is a couple of months alone, to get her book and life together. She figured a remote cabin in the upper peni
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