Postaxial acrofacial dysostosis or Miller syndrome - A case report

D. Barbuti, C. Orazi, A. Reale, C. Paradisi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A case of postaxial acrofacial dysostosis (Miller syndrome) is presented. This rare syndrome is essentially characterized by a Treacher - Collins-like facial appearance together with absence of the fifth digital ray of all limbs and variable forearm hypoplasia.

Original languageEnglish
Pages (from-to)445-446
Number of pages2
JournalEuropean Journal of Pediatrics
Volume148
Issue number5
DOIs
Publication statusPublished - Feb 1989

Fingerprint

Forearm
Extremities
Genee-Wiedemann syndrome

Keywords

  • Limb anomalies
  • Postaxial acrofacial dysostosis

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Postaxial acrofacial dysostosis or Miller syndrome - A case report. / Barbuti, D.; Orazi, C.; Reale, A.; Paradisi, C.

In: European Journal of Pediatrics, Vol. 148, No. 5, 02.1989, p. 445-446.

Research output: Contribution to journalArticle

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