P

 

Pierre Robin sendromu

Nedeni? - AR?

Riboflavin eksikliğine bağlı olduğu sanılmakta

Pierre Robin sequence bulguları

Uvula bifida

Prematüre dişler (erken sürme)

Ankyloglossia

Yutma refleksi ve solunum güçlüğü

Hidrosefalus

Zeka geriliği

Cor pulmonale ile sonlanan kalp anomalileri

Natal solunum güçlüğü

Ekstremite anomalileri (konjenital)

Ekstremite ampütasyonları (konjenital)

Göz ve kulak defektleri

Yineleyen kulak infeksiyonları

Spina bifida

 

  • Elliott MA, Studen-Pavlovich DA, Ranalli DN. Prevalence of selected pediatric conditions in children with Pierre Robin sequence. Pediatric Dentistry, 17(2):106-111, 1995

  • Laitinen SH, Heliövaara A, Ranta RE. Craniofacial morphology in young adults with the Pierre Robin Sequence and Isolated Cleft Palate, Acta Odontologica Scandinavica, 55:4, 223-228, 1997

  • Wilcox BK, Tatum SA. Cerebro-costo-mandibular syndrome presenting as Pierre Robin sequence. American Journal of Otolaryngology, 25(4):258-262, 2004

  • Mackay DR. Controversies in the diagnosis and management of the Robin sequence. Journal of Craniofacial Surgery, 22(2):415-420, 2011

  • Tan TY, Farlie PG. Rare syndromes of the head and face-Pierre Robin sequence. Wiley Interdisciplinary Reviews: Developmental Biology, 2(3):369-377, 2013

  • Tan TY, Kilpatrick N, Farlie PG. Developmental and genetic perspectives on Pierre Robin sequence. Americam Journal of Medical Genetics C, 163C: 295-305, 2013

  • Gordon CT, Attanasio C, Bhatia S, et al. Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence. Human Mutation, 35(8): 1011-1020, 2014

  • Côté A, Fanous A, Almajed A, Lacroix Y. Pierre Robin sequence: review of diagnostic and treatment challenges. International Journal of Pediatric Otorhinolaryngology, 79(4):451-464, 2015

  • Bütow K-W, Zwahlen RA, Morkel JA, Naidoo S. Pierre Robin sequence: Subdivision, data, theories, and treatment – Part 2: Syndromic and nonsyndromic Pierre Robin sequence. Annals of Maxillofacial Surgery, 6(1): 35–37, 2016