Coexistence of oto-palato-digital syndrome type II and Arnold-Chiari I malformation in an infant

Po Cheng Hung, Huei Shyong Wang, Tai Ngar Lui

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

A Taiwanese infant with clinically apparent oto-palato-digital syndrome type II had Arnold-Chiari I malformation. Arnold-Chiari I malformation has not been reported previously to occur in association with oto-palato-digital type II syndrome. The pathogenesis of both conditions has remain unclear although the Arnold-Cliari I malformation is most likely due to a developmental abnormality of improperly times or incomplete closure of the neural tube. We propose the physician who care for children with OPD type II must be aware of one more condition Copyright (C) 1999 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)488-490
Number of pages3
JournalBrain and Development
Volume21
Issue number7
DOIs
Publication statusPublished - Oct 1 1999
Externally publishedYes

Fingerprint

Arnold-Chiari Malformation
Neural Tube
Child Care
Physicians

Keywords

  • Arnold-Chiari malformation
  • Oto-palato-digital syndrome

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health
  • Neurology

Cite this

Coexistence of oto-palato-digital syndrome type II and Arnold-Chiari I malformation in an infant. / Hung, Po Cheng; Wang, Huei Shyong; Lui, Tai Ngar.

In: Brain and Development, Vol. 21, No. 7, 01.10.1999, p. 488-490.

Research output: Contribution to journalArticle

Hung, Po Cheng ; Wang, Huei Shyong ; Lui, Tai Ngar. / Coexistence of oto-palato-digital syndrome type II and Arnold-Chiari I malformation in an infant. In: Brain and Development. 1999 ; Vol. 21, No. 7. pp. 488-490.
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