Epidermolysis bullosa, pyloric atresia, aplasia cutis congenita: Histopathological delineation of an autosomal recessive disease
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference39 articles.
1. Aplasia cutis congenita associated with epidermolysis bullosa and pyloric atresia: The diagnostic role of prenatal ultrasonography
2. An unusual case of epidermolysis bullosa hereditaria letalis with cutaneous scarring and pyloric atresia
3. Birth Defects;Bauer,1981
4. (1979): The mechanobullous diseases (epidermolysis bullosa) In (eds): ?Dermatology in General Medicine,? 2nd Ed. New York: McGraw-Hill, pp. 334-347.
5. Jenctlonal Epidermolysis Bullosa, Pyloric Atresia, and Genitourinary Disease
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1. Bart Syndrome Associated with Pyloric Atresia: An Uncommon Case Report;INT J PEDIATR-MASSHA;2023
2. Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1;Frontiers in Genetics;2022-04-01
3. Novel compound heterozygous ITGB4 mutations underlie lethal junctional epidermolysis bullosa with pyloric atresia and aplasia cutis congenita;The Journal of Dermatology;2022-01-11
4. Case Report: Uncommon Association of ITGB4 and KRT10 Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita;Frontiers in Genetics;2021-07-08
5. Epidermolysis bullosa with congenital absence of skin: Review of the literature;Pediatric Dermatology;2020-07-20
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