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J Pediatr ; 193: 261-264.e1, 2018 02.
Article in English | MEDLINE | ID: mdl-29198538

ABSTRACT

We report a case of nonfatal junctional epidermolysis bullosa and pyloric atresia in a newborn. We identified a substitution (c.914C>T) for the integrin ß4 gene that has been associated with favorable outcome. A novel mutation (c.2011T>G) of unknown significance was also found in this patient who is now thriving.


Subject(s)
Epidermolysis Bullosa, Junctional/genetics , Gastric Outlet Obstruction/genetics , Integrin beta4/genetics , Pylorus/abnormalities , Epidermolysis Bullosa, Junctional/complications , Epidermolysis Bullosa, Junctional/diagnosis , Female , Gastric Outlet Obstruction/complications , Gastric Outlet Obstruction/surgery , Heterozygote , Humans , Infant, Newborn , Laparotomy/methods , Mutation , Pylorus/surgery , Plastic Surgery Procedures/methods , Skin/pathology
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