Literature DB >> 18977702

What is 'Pierre Robin sequence'?

C C Breugem1, A B Mink van der Molen.   

Abstract

Different nosology has hampered our understanding of patients with Robin sequence. Defining this disorder correctly has important consequences for physicians and parents. While reviewing treatment options for Robin sequence we were surprised to see how often different definitions were used to describe this condition. This prompted us to perform a review into the current understanding when diagnosing and defining this disorder. At our Annual Dutch Cleft Palate Meeting a questionnaire was given to all those attending requesting them to summarise characteristics needed for a definition of 'Robin sequence'. Sixty-six questionnaires were returned, demonstrating 29 different descriptions. Our study demonstrates that there is widespread confusion in the Netherlands defining Robin sequence. This lack of uniformity in the definition hampers the comparison of outcome studies. The treatment of patients with Robin sequence often involves multidisciplinary involvement, making it crucial to have one common definition. We suggest using the description originally summarised by Pierre Robin consisting of micrognathia, glossoptosis and airway compromise. Once the diagnosis of Robin sequence is made other adjuncts such as an associated cleft palate, syndrome or feeding problems could be added to the description.

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Mesh:

Year:  2008        PMID: 18977702     DOI: 10.1016/j.bjps.2008.06.050

Source DB:  PubMed          Journal:  J Plast Reconstr Aesthet Surg        ISSN: 1748-6815            Impact factor:   2.740


  12 in total

1.  Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study.

Authors:  Sushil Kumar Jaiswal; Krishna Kishore Sukla; Vineeta Gupta; Amit Kumar Rai
Journal:  J Genet       Date:  2014-12       Impact factor: 1.166

2.  Percutaneous gastrostomy tubes in children with Pierre Robin sequence: efficacy, maintenance and complications.

Authors:  Hyder Al-Attar; Arvind K Shergill; Nicole E Brown; Cindy Guernsey; David Fisher; Michael Temple; Philip John; Joao G Amaral; Dimitri Parra; Bairbre L Connolly
Journal:  Pediatr Radiol       Date:  2011-12-01

3.  Bilateral mandibular distraction osteogenesis in the neonate with pierre robin sequence and airway obstruction: a primary option.

Authors:  Horácio Zenha; Luis Azevedo; Leonor Rios; Alberto Pereira; Armindo Pinto; Maria Luz Barroso; Horácio Costa
Journal:  Craniomaxillofac Trauma Reconstr       Date:  2012-03

Review 4.  A systematic review on the outcome of mandibular distraction osteogenesis in infants suffering Robin sequence.

Authors:  Emma C Paes; Aebele B Mink van der Molen; Marvick S M Muradin; Lucienne Speleman; Frea Sloot; Moshe Kon; Corstiaan C Breugem
Journal:  Clin Oral Investig       Date:  2013-05-31       Impact factor: 3.573

5.  A pragmatic approach to infants with Robin sequence: a retrospective cohort study and presence of a treatment algorithm.

Authors:  Emma C Paes; Daan P F van Nunen; Lucienne Speleman; Marvick S M Muradin; Bram Smarius; Moshe Kon; Aebele B Mink van der Molen; Aebele B Mink van der Molen; Titia L E M Niers; Esther S Veldhoen; Corstiaan C Breugem
Journal:  Clin Oral Investig       Date:  2015-02-15       Impact factor: 3.573

6.  Mortality in Robin sequence: identification of risk factors.

Authors:  Robrecht J H Logjes; Maartje Haasnoot; Petra M A Lemmers; Mike F A Nicolaije; Marie-José H van den Boogaard; Aebele B Mink van der Molen; Corstiaan C Breugem
Journal:  Eur J Pediatr       Date:  2018-02-28       Impact factor: 3.183

7.  Birth prevalence and initial treatment of Robin sequence in Germany: a prospective epidemiologic study.

Authors:  Scarlet Vatlach; Christoph Maas; Christian F Poets
Journal:  Orphanet J Rare Dis       Date:  2014-01-17       Impact factor: 4.123

8.  Pierre Robin sequence: Subdivision, data, theories, and treatment - Part 1: History, subdivisions, and data.

Authors:  Kurt-W Bütow; Roger Arthur Zwahlen; Jean A Morkel; Sharan Naidoo
Journal:  Ann Maxillofac Surg       Date:  2016 Jan-Jun

9.  Late detection of cleft palate.

Authors:  K H Hanny; I A C de Vries; S J Haverkamp; K P Q Oomen; W M Penris; M J C Eijkemans; M Kon; A B Mink van der Molen; C C Breugem
Journal:  Eur J Pediatr       Date:  2015-08-01       Impact factor: 3.183

10.  A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report.

Authors:  Maoying Jiang; Shanlin Wang; Fei Li; Juan Geng; Yiting Ji; Ke Li; Xiaodong Jiang
Journal:  Medicine (Baltimore)       Date:  2020-11-06       Impact factor: 1.817

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