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Rectal atresia as distinguished from rectal agenesis

โœ Scribed by Ruth V. Magnus


Book ID
118334867
Publisher
Elsevier Science
Year
1968
Tongue
English
Weight
425 KB
Volume
3
Category
Article
ISSN
0022-3468

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A newborn boy presented with bilateral split handfoot malformation, sparse hair, dry and scaly skin, and nasolacrimal duct obstruction. Despite absence of cleft lip or palate, the findings fit the EEC syndrome. Additionally, the boy had rectal atresia. At least six further patients with