Guest guest Posted August 31, 2004 Report Share Posted August 31, 2004 This is a research abstract from Kaohsiung J Med Sci. 2001 Sep;17(9):484-8. (HMSN is CMT) Superior mesenteric artery syndrome associated with hereditary motor and sensory neuropathy type II--a case report. Lin LC, Lee IH, Yang RC, Jong YJ. Department of Pediatrics, College of Medicine, Kaohsiung Medical University, No. 100, Shih-Chuan 1st Rd., Kaohsiung 80708, Taiwan. A 14-year-old girl with superior mesenteric artery (SMA) syndrome associated with hereditary motor and sensory neuropathy (HMSN) type II is reported. The initial presentations of HMSN type II were developmental delay and gait disturbance at 2 years of age. All deep tendon reflexes were absent. Nerve conduction velocities and left sural nerve biopsy all revealed axonal changes. Recently, she suffered from intermittent bilious vomiting and epigastralgia for 6 months. That caused body weight loss from 40 kg to 28 kg. Abdominal echography showed narrowed superior mesenteric artery angle. Upper gastrointestinal series revealed obstruction of third portion of duodenum. Accordingly, SMA syndrome was diagnosed. To the best of our knowledge, this case is the first report of SMA with HMSN type II in the world. When a child with chronic neurological disease presents with intermittent vomiting, SMA should be considered as a disease entity of differential diagnosis. ******************************************* here is another link that mentions superior mesenteric artery syndrome at the end. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve & db=pubmed & dopt=Abstra\ ct & list_uids=3955951 Quote Link to comment Share on other sites More sharing options...
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