A 2990-g, full-term, baby girl with multiple congenital anomalies was born to a G4P2 mother.
Three-dimensional CT reconstructions of the mandible (Figures 1, A and B) reveal prominent retromicrognathia. Note the zygomatic arch and external auditory canal are preserved. Sagittal NECT (Figure 2) demonstrates glossoptosis (ie, posteroinferior displacement of the tongue, causing obstruction of the oropharynx). The hard palate is shortened in length. The patient subsequently underwent glossopexy to advance the tongue. Axial NECT (Figure 3) shows U-shaped cleft palate. KUB (Figure 4) performed on Day 2 of life demonstrates three things: 1) segmentation of the posterior ribs with apparent pseudoarthroses; 2)10 paired ribs; and 3) age-appropriate bone mineralization.
Pierre Robin sequence (PRSe).
Differential diagnosis includes velocardiofacial syndrome (Shprintzen-Goldberg syndrome), Stickler syndrome, and Treacher-Collins syndrome (mandibulofacial dysostosis).
An important step in approaching syndromes of the first and second branchial arches is identification of defects, including cleft lip with or without cleft palate, micrognathia and atresia of the external auditory canal.1,2 Isolated Pierre Robin syndrome (PRS) is a triad comprising retromicrognathia, glossoptosis and posterior U-shaped cleft.3 The term “sequence” [PRSe] is sometimes applied in reference to the idea that many of the phenotypic manifestations are the result of an initial anomaly; ie, a small jaw that then leads to a posteriorly displaced tongue and cleft palate. The skeletal anomalies in our case, specifically the segmentation and rib anomalies, are not specific to PRSe, which is diagnosed with associated syndromes in almost half of cases.4
PRSe has been associated with changes to the Sex Determining Region Y-box 9 (SOX9) gene, which encodes for a transcription factor protein that plays a critical role in skeletal and reproductive development.5 It is typically not an inherited disorder but rather occurs de novo due to genetic mutation, although a small subset has been reported with a known family history.4
Given their oropharyngeal abnormalities, children with the Pierre Robin sequence often undergo gastrostomy tube placement to meet their nutritional needs.1 In 2012 a Paris-based group published results of a longitudinal prospective study on children with Pierre Robin syndrome suggesting a good prognosis with no significant cognitive deficits but with diminished language skills.6 Eating behavior improved over time with only 6% of children reporting eating behavioral difficulties by age 6.
The Pierre Robin syndrome is a good illustration of the consequences of a single in-utero malformation leading to a series of anatomic abnormalities with several associated clinical manifestations. Early identification of retromicrognathia suggests that the clinician look closely for associated abnormalities and anticipate care needs with particular attention to feeding and airway needs. The prognosis of these children is good with no long-term cognitive deficits and progressive improvement of oropharyngeal feeding behaviors.
Pierre Robin sequence. Appl Radiol.
Prepared by Dr. Sugi while at the Department of Radiology, Mayo Clinic, Scottsdale, AZ; Dr. Jorgensen, while at the Department of Medical Imaging, Phoenix Children’s Hospital, Phoenix, AZ; Dr. A. Towbin, while at the Department of Radiology, Children’s Hospital Medical Center, Cincinnati, OH; and Dr. R. Towbin, while at the Department of Medical Imaging, Phoenix Children’s Hospital, Phoenix, AZ.