Literature DB >> 1151545

U-shaped palatal defect in the Robin anomalad: developmental and clinical relevance.

J W Hanson, D W Smith.   

Abstract

The palatal defect in patients with the Robin anomalad was found to be U shaped. This finding is compatible with the hypothesis that the underlying dysmorphic event is usually early mandibular hypoplasia with secondary extrinsic obstruction of palatal closure by a posteriorly displaced tongue. The more common V-shaped defects of palate closure arise by a different mechanism. Unfortunately, available recurrence risk data for cleft palate do not allow for this distinction. Furthermore, physicians should be alert for instances in which the Robin anomalad is but one feature of a broader pattern of malformation. In the current study, 25% of the 28 patients ascertained as having the Robin anomalad had a recognizable syndrome for which specific, but varying, genetic counsel was indicated.

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Year:  1975        PMID: 1151545     DOI: 10.1016/s0022-3476(75)80063-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  11 in total

1.  Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies.

Authors:  Jessie X Xu; Nicky Kilpatrick; Naomi L Baker; Anthony Penington; Peter G Farlie; Tiong Yang Tan
Journal:  Mol Syndromol       Date:  2016-09-15

2.  The influence of the Tübingen soft palate plate and early cleft closure on the nasopharyngeal airway for the management of airway obstruction in an infant with Pierre Robin sequence: A case report.

Authors:  Lucia Gerzanic; Matthias Feichtinger; Hans Kärcher
Journal:  Int J Surg Case Rep       Date:  2012-08-31

Review 3.  Robin sequence: from diagnosis to development of an effective management plan.

Authors:  Kelly N Evans; Kathleen C Sie; Richard A Hopper; Robin P Glass; Anne V Hing; Michael L Cunningham
Journal:  Pediatrics       Date:  2011-04-04       Impact factor: 7.124

4.  Congenital malformations associated with anencephaly and iniencephaly.

Authors:  T J David; A Nixon
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

5.  766 cases of oral cleft in Italy. Data from Emilia Romagna (IMER) and northeast Italy (NEI) registers.

Authors:  M Milan; G Astolfi; S Volpato; G P Garani; M Clementi; R Tenconi; S Boni; E Calzolari
Journal:  Eur J Epidemiol       Date:  1994-06       Impact factor: 8.082

6.  The Robin anomalad (Pierre Robin syndrome)--a follow up study.

Authors:  A J Williams; M A Williams; C A Walker; P G Bush
Journal:  Arch Dis Child       Date:  1981-09       Impact factor: 3.791

7.  Polysomnographic findings in infants with Pierre Robin sequence.

Authors:  Abdullah Khayat; Saadoun Bin-Hassan; Suhail Al-Saleh
Journal:  Ann Thorac Med       Date:  2017 Jan-Mar       Impact factor: 2.219

8.  Severity of Retrognathia and Glossoptosis Does Not Predict Respiratory and Feeding Disorders in Pierre Robin Sequence.

Authors:  Anne Morice; Véronique Soupre; Delphine Mitanchez; Francis Renault; Brigitte Fauroux; Sandrine Marlin; Nicolas Leboulanger; Natacha Kadlub; Marie-Paule Vazquez; Arnaud Picard; Véronique Abadie
Journal:  Front Pediatr       Date:  2018-11-20       Impact factor: 3.418

9.  Long-term Speech Outcomes of Cleft Palate Repair in Robin Sequence versus Isolated Cleft Palate.

Authors:  Robrecht J H Logjes; Susanna Upton; Bryce A Mendelsohn; Ryan K Badiee; Corstiaan C Breugem; William Y Hoffman; Jason H Pomerantz
Journal:  Plast Reconstr Surg Glob Open       Date:  2021-01-21

Review 10.  Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex.

Authors:  Susan M Motch Perrine; Meng Wu; Greg Holmes; Bryan C Bjork; Ethylin Wang Jabs; Joan T Richtsmeier
Journal:  J Dev Biol       Date:  2020-12-05
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