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Pierre Robin-like syndrome

MedGen UID:
894004
•Concept ID:
CN239861
•
Disease or Syndrome

Professional guidelines

PubMed

Treatment of upper airway obstruction and feeding problems in Robin-like phenotype.
Poets CF, Bacher M
J Pediatr 2011 Dec;159(6):887-92. Epub 2011 Aug 31 doi: 10.1016/j.jpeds.2011.07.033. PMID: 21885059

Recent clinical studies

Diagnosis

Incidence of maxillofacial involvement in arthrogryposis multiplex congenita.
Steinberg B, Nelson VS, Feinberg SE, Calhoun C
J Oral Maxillofac Surg 1996 Aug;54(8):956-9. doi: 10.1016/s0278-2391(96)90391-2. PMID: 8765384

Prognosis

Incidence of maxillofacial involvement in arthrogryposis multiplex congenita.
Steinberg B, Nelson VS, Feinberg SE, Calhoun C
J Oral Maxillofac Surg 1996 Aug;54(8):956-9. doi: 10.1016/s0278-2391(96)90391-2. PMID: 8765384

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      Related medical variations

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