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Article

Clinical outcomes and molecular profile of patients with Carmi syndrome: A systematic review and evidence quality assessment.

Journal of pediatric surgery - 1 Jul 2019

Mylonas Konstantinos S, Hayes Meaghan, Ko Lauren N, Griggs Cornelia L, Kroshinsky Daniela, Masiakos Peter T

Abstract excerpt

PURPOSE: Carmi syndrome is a rare genetic disorder characterized by junctional epidermolysis bullosa (JEB) and pyloric atresia (PA). We reviewed the clinicopathologic and molecular features of patients with Carmi syndrome to identify predictors of clinical outcome and guide surgical PA repair. METHODS: A PRISMA-compliant systematic literature review of PubMed, CINAHL, and the Cochrane Library was performed....

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PMID: 29935895
DOI: 10.1016/j.jpedsurg.2018.05.019

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