Skip to search formSkip to main contentSkip to account menu

Congenital pyloric atresia

Congenital atresia of the pylorus. [HPO:probinson]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2007
Review
2007
  • A. Al-Salem
  • Pediatric Surgery International
  • 2007
  • Corpus ID: 8735585
Congenital pyloric atresia (CPA) is a very rare condition that was first described by Calder in 1749. Commonly, CPA occurs as an… 
2002
2002
Congenital pyloric atresia (CPA) is a very rare malformation. It can occur as an isolated lesion or in association with other… 
2002
2002
Although congenital pyloric atresia commonly occurs in isolation, it has rarely been reported in association with other… 
Highly Cited
2001
Highly Cited
2001
Epidermolysis bullosa with pyloric atresia (EB-PA: OMIM 226730), also known as Carmi syndrome, is a rare autosomal recessive… 
Review
1999
Review
1999
  • A. Al-Salem
  • Pediatric Surgery International
  • 1999
  • Corpus ID: 20845730
Abstract A case of congenital pyloric atresia associated with duodenal atresia, jejunal atresia, and a duplication is described… 
Highly Cited
1998
Highly Cited
1998
Epidermolysis bullosa with pyloric atresia (EB-PA), an autosomal recessive genodermatosis, manifests with neonatal cutaneous… 
1998
1998
Mutations in the genes encoding the subunit polypeptides of the alpha6beta4 integrin (ITGA6 and ITGB4, respectively) have been… 
1992
1992
Familial congenital pyloric atresia is a rare malformation of the fetal gastrointestinal tract. It usually manifests as maternal… 
Review
1981
Review
1981
A 32-week-old (gestational age) female infant with epidermolysis bullosa letalis (EBL) (confirmed by light and electron… 
1973
1973
Congenital pyloric atresia is a very rare condition and, to our knowledge, has never been described in siblings. Two siblings (a…