LA SINDROME EEC. DESCRIZIONE DI DUE CASI IN UNA STESSA FAMIGLIA

Translated title of the contribution: EEC syndrome: description of two cases in the same family

G. Gemme, E. Bonioli, G. Ruffa, P. Grosso

Research output: Contribution to journalArticlepeer-review

Abstract

Two cases of the EEC syndrome in children of the same family, only one observed directly, are reported. The case presented the complete picture, i.e., ectodermic dysplasia, ectodactylia and labiopalatoschisis as well as psychomotor retardation. This malformative picture is extremely rare and only about ten cases have been reported in the world literature. On the basis of the known consanguinity of the parents, a recessive autosomic transmission hypothesis is advanced.

Translated title of the contributionEEC syndrome: description of two cases in the same family
Original languageItalian
Pages (from-to)36-43
Number of pages8
JournalMinerva Pediatrica
Volume28
Issue number1
Publication statusPublished - 1976

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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