The Richieri-Costa and Pereira syndrome: report of two Brazilian siblings and review of literature

Am J Med Genet A. 2011 May;155A(5):1173-7. doi: 10.1002/ajmg.a.33975. Epub 2011 Apr 11.

Abstract

Richieri-Costa and Pereira syndrome is a rare autosomal recessive disorder characterized specially by Pierre Robin sequence with cleft mandible and limb anomalies. There are a typical laryngeal anomaly which encompass short and round larynx, absent or abnormal epiglottis, and abnormal aryepiglottic folds. Most patients reported were from Brazil. We describe a brother and sister with Richieri-Costa and Pereira syndrome on another Brazilian family documenting their physical findings and laryngeal defects. We also review the literature and discuss the main clinical characteristics and etiology.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child, Preschool
  • Clubfoot* / diagnosis
  • Clubfoot* / pathology
  • Female
  • Hand Deformities, Congenital* / diagnosis
  • Hand Deformities, Congenital* / pathology
  • Humans
  • Infant
  • Male
  • Pierre Robin Syndrome* / diagnosis
  • Pierre Robin Syndrome* / pathology
  • Siblings*
  • Syndrome

Supplementary concepts

  • Richieri Costa Pereira syndrome