Nager syndrome

A congenital malformation syndrome characterized by mandibulofacial dystosis (malar hypoplasia, micrognathia, external ear malformations) and variable preaxial limb defects.

Pierre-Robin sequence

Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate.


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(per page)
PMID (PMCID)
27723379
 FEMALE Infant, Newborn
A Case Report of Absent Epiglottis in Children With Nager Syndrome: Its Impact on Swallowing.
Tay SY, Loh WS, Lim TC.
Cleft Palate Craniofac J. 2017;54(6):754-757.
Nager syndrome has previously been described in children with Pierre Robin sequence and other syndromes.
25808856
 MALE Infant, Newborn
Nager syndrome and Pierre Robin sequence.
Rosa RF, Guimaraes VB, Beltrao LA, Trombetta JS, Lliguin KL, de Mattos VF, Zen PR.
Pediatr Int. 2015;57(2):e69-72.
The present patient had typical findings of Nager syndrome and Pierre Robin sequence.
25808856
 MALE Infant, Newborn
Nager syndrome and Pierre Robin sequence.
Rosa RF, Guimaraes VB, Beltrao LA, Trombetta JS, Lliguin KL, de Mattos VF, Zen PR.
Pediatr Int. 2015;57(2):e69-72.
Nager syndrome and Pierre Robin sequence.
26228803
 FEMALE Infant
[Nager syndrome associated with tetralogy of Fallot: A frequent association?].
Bellanger C, Villedieu F, Gerard M, Guillois B.
Arch Pediatr. 2015;22(9):974-7.
We report the case of a child who had a characteristic association (Pierre Robin sequence, bilateral and symmetrical malar hypoplasia, absent thumbs) clinically diagnosed as Nager syndrome.
22097658
 MIXED_SAMPLE Infant, Newborn
[Mandibular distraction osteogenesis in patients with craniofacial malformation].
Maranes Galvez C, Martinez Plaza A, Fernandez Valades R, Liceras Liceras E, Martin Cano F, Cortes Sanchez R, Martinez Telleria A, Cabello A, Garcia Medina B.
Cir Pediatr. 2011;24(2):102-8.
Craniofacial malformations (Pierre-Robin sequence, Treacher-Collins syndrome, Nager syndrome, etc.)
11103674
 MIXED_SAMPLE
[Distraction osteogenesis of the mandible in 2 children with obstruction of the upper respiratory tract due to micrognathia].
Becking AG, Jansma J.
Ned Tijdschr Geneeskd. 2000;144(44):2111-5.
A girl approximately 2 years old with Pierre Robin sequence had periods of nocturnal respiratory insufficiency as a consequence of micrognathia and a boy nearly 4 years old with Nager syndrome and tracheostomy was retarded in his speech development, had problems swallowing and often had respiratory tract infections.