Junctional epidermolysis bullosa associated with congenital localized absence of skin, and pyloric atresia in two newborn siblings
- 1 February 2001
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 44 (2) , 330-335
- https://doi.org/10.1067/mjd.2001.105480
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Gastric outlet obstruction and epidermolysis bullosaJournal of the American Academy of Dermatology, 1997
- Epidermolysis bullosa associated with pyloric, esophageal, and anal atresia: A case reportJournal of Pediatric Surgery, 1995
- Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one familyPrenatal Diagnosis, 1995
- Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresiaNature Genetics, 1995
- Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosaNature Genetics, 1994
- Congenital gastric outlet obstructionJournal of Pediatric Surgery, 1989
- Aplasia cutis congenita: A clinical review and proposal for classificationJournal of the American Academy of Dermatology, 1986
- Bart's Syndrome: Microscopic, Ultrastructural, and Immunofluorescent Mapping FeaturesPediatric Dermatology, 1986
- Dystrophic epidermolysis bullosa presenting with congenital localized absence of skin: report of four casesBritish Journal of Dermatology, 1983
- PRENATAL DIAGNOSIS OF EPIDERMOLYSIS BULLOSA LETALISPublished by Elsevier ,1980