eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pierre robin sequence |
| Comorbidity | C0008925|cleft palate |
| Sentences | 6 |
| PubMedID- 23619496 | pierre-robin syndrome presents with micrognathia, cleft palate and glossoptosis. |
| PubMedID- 22851992 | cleft palate patients with ankyloglossia syndrome, pierre-robin syndrome, stickler syndrome, chromosomal anomalies and kabuki make-up syndrome were excluded from the study. |
| PubMedID- 21121765 | In older children (t2: 10 to 13 years) mandibular length was significantly shorter in the pierre robin sequence group compared with the isolated cleft palate group (difference = 10.9 mm, p = .009). |
| PubMedID- 25554857 | Objective: to describe pierre robin sequence patients with a cleft palate from a multidisciplinary perspective. |
| PubMedID- 22420397 | Results: the relative risk of a difficult intubation in the cleft lip, cleft palate without the pierre robin sequence, cleft lip-palate, and cleft palate with pierre robin sequence groups was 0, 2.7, 10, and 23%, respectively. |
| PubMedID- 20301724 | Campomelic dysplasia (cd) is a skeletal dysplasia characterized by distinctive facies, pierre robin sequence with cleft palate, shortening and bowing of long bones, and club feet. |
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