Unusual cranial aspects of the Apert syndrome

M. M. Cohen, S. Kreiborg

Research output: Contribution to journalReview articlepeer-review

23 Citations (Scopus)

Abstract

Frank cloverleaf skull is found in approximately 4% of Apert-syndrome infants. However, the usual Apert skull and its cloverleaf form are spectral in nature. In all patients, the temporal bones are obliquely situated, and the degree to which this is so determines whether no, mild, moderate, or severe cloverleafing will occur. True encephalocele rarely is found in the Apert syndrome, but pseudoencephl alocele in the frontal region sometimes is confused with it. Because the Apert calvaria at birth is characterized by a widely gaping midline defect, the midfrontal region of the brain is not covered by bone during early infancy. However, with time, closure of the midline defect occurs by coalescence of bony islands, thus covering the pseudoencephalic region. Also discussed in this paper are (a) atypical calvarial development with patency of the coronal sutures in one case, (b) size and position of the temporal muscles, and (c) size and position of the superficial temporal fat pads.

Original languageEnglish
Pages (from-to)48-56
Number of pages9
JournalJournal of Craniofacial Genetics and Developmental Biology
Volume14
Issue number1
Publication statusPublished - 1994

ASJC Scopus Subject Areas

  • Genetics
  • Developmental Biology

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