Syndromic foramina parietalia permagna

Am J Med Genet. 1998 Aug 6;78(5):401-5. doi: 10.1002/(sici)1096-8628(19980806)78:5<401::aid-ajmg1>3.0.co;2-o.

Abstract

We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of branchial and auricular fistulae, abnormal face, and skeletal abnormalities including foramina parietalia permagna.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple* / diagnostic imaging
  • Ear / abnormalities
  • Face / abnormalities
  • Genitalia, Male / abnormalities
  • Hand Deformities, Congenital / diagnostic imaging
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Male
  • Mouth Abnormalities
  • Parietal Bone / abnormalities*
  • Parietal Bone / diagnostic imaging
  • Phenotype
  • Radiography
  • Scoliosis / diagnostic imaging
  • Syndrome
  • Toes / abnormalities