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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 1
1975 1
1978 3
1979 1
1980 1
1982 1
1983 4
1985 1
1987 7
1988 6
1989 7
1990 8
1991 9
1992 11
1993 9
1994 7
1995 10
1996 9
1997 8
1998 9
1999 13
2000 7
2001 7
2002 8
2003 4
2004 17
2005 13
2006 8
2007 9
2008 6
2009 8
2010 9
2011 15
2012 20
2013 7
2014 17
2015 13
2016 15
2017 8
2018 12
2019 6
2020 15
2021 17
2022 10
2023 19
2024 7

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Search Results

370 results

Results by year

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Page 1
Pierre Robin Sequence.
Hsieh ST, Woo AS. Hsieh ST, et al. Clin Plast Surg. 2019 Apr;46(2):249-259. doi: 10.1016/j.cps.2018.11.010. Epub 2019 Feb 8. Clin Plast Surg. 2019. PMID: 30851756 Review.
Pierre Robin sequence consists of clinical triad of micrognathia, glossoptosis, and airway compromise with variable inclusion of cleft palate. ...
Pierre Robin sequence consists of clinical triad of micrognathia, glossoptosis, and airway compromise with variable inclusion of clef …
Treacher Collins Syndrome: Genetics, Clinical Features and Management.
Marszałek-Kruk BA, Wójcicki P, Dowgierd K, Śmigiel R. Marszałek-Kruk BA, et al. Genes (Basel). 2021 Sep 9;12(9):1392. doi: 10.3390/genes12091392. Genes (Basel). 2021. PMID: 34573374 Free PMC article. Review.
Features of TCS include microtia with conductive hearing loss, slanting palpebral fissures with possibly coloboma of the lateral part of lower eyelids, midface hypoplasia, micrognathia as well as sporadically cleft palate and choanal atresia or stenosis. ...
Features of TCS include microtia with conductive hearing loss, slanting palpebral fissures with possibly coloboma of the lateral part of low …
Cri du Chat syndrome.
Cerruti Mainardi P. Cerruti Mainardi P. Orphanet J Rare Dis. 2006 Sep 5;1:33. doi: 10.1186/1750-1172-1-33. Orphanet J Rare Dis. 2006. PMID: 16953888 Free PMC article. Review.
The main clinical features are a high-pitched monochromatic cry, microcephaly, broad nasal bridge, epicanthal folds, micrognathia, abnormal dermatoglyphics, and severe psychomotor and mental retardation. ...
The main clinical features are a high-pitched monochromatic cry, microcephaly, broad nasal bridge, epicanthal folds, micrognathia, ab …
Developmental maxillofacial anomalies.
Baxter DJ, Shroff MM. Baxter DJ, et al. Semin Ultrasound CT MR. 2011 Dec;32(6):555-68. doi: 10.1053/j.sult.2011.06.004. Semin Ultrasound CT MR. 2011. PMID: 22108218 Review.
This review article provides an overview of maxillofacial embryogenesis, clinical symptoms, and characteristic imaging features of several anomalies, including choanal atresia, congenital nasal piriform aperture stenosis, dacryocystoceles, nasolacrimal duct stenosis, cleft lip an …
This review article provides an overview of maxillofacial embryogenesis, clinical symptoms, and characteristic imaging features of several a …
Hearing Loss in Stickler Syndrome: An Update.
Acke FRE, De Leenheer EMR. Acke FRE, et al. Genes (Basel). 2022 Sep 1;13(9):1571. doi: 10.3390/genes13091571. Genes (Basel). 2022. PMID: 36140739 Free PMC article. Review.
Its main symptoms are high myopia, retinal detachment, joint hypermobility, early osteoarthritis, cleft palate, midfacial hypoplasia, micrognathia and hearing loss. Large phenotypical variability is apparent and partly explained by the underlying genetic heterogeneity, inc …
Its main symptoms are high myopia, retinal detachment, joint hypermobility, early osteoarthritis, cleft palate, midfacial hypoplasia, mic …
Human facial dysostoses.
Wieczorek D. Wieczorek D. Clin Genet. 2013 Jun;83(6):499-510. doi: 10.1111/cge.12123. Epub 2013 Apr 8. Clin Genet. 2013. PMID: 23565775 Review.
The craniofacial anomalies shared by the two groups consist of downslanting palpebral fissures, coloboma of the lower eyelid, from which the eyelashes medial to the defect may be absent, hypoplasia of the zygomatic complex, micrognathia, and microtia, which is often associ …
The craniofacial anomalies shared by the two groups consist of downslanting palpebral fissures, coloboma of the lower eyelid, from which the …
Glossoptosis.
Schweiger C, Manica D, Kuhl G. Schweiger C, et al. Semin Pediatr Surg. 2016 Jun;25(3):123-7. doi: 10.1053/j.sempedsurg.2016.02.002. Epub 2016 Feb 18. Semin Pediatr Surg. 2016. PMID: 27301596 Review.
Glossoptosis causes varying degrees of airway obstruction and feeding difficulties. It can occur as a consequence of micrognathia in Robin Sequence, but can also occur in children with hypotonia. ...
Glossoptosis causes varying degrees of airway obstruction and feeding difficulties. It can occur as a consequence of micrognathia in …
Meier-Gorlin syndrome.
de Munnik SA, Hoefsloot EH, Roukema J, Schoots J, Knoers NV, Brunner HG, Jackson AP, Bongers EM. de Munnik SA, et al. Orphanet J Rare Dis. 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x. Orphanet J Rare Dis. 2015. PMID: 26381604 Free PMC article. Review.
Analysis of the Relationship Between Micrognathia and Cleft Palate: A Systematic Review.
Price KE, Haddad Y, Fakhouri WD. Price KE, et al. Cleft Palate Craniofac J. 2016 Mar;53(2):e34-44. doi: 10.1597/14-238. Epub 2015 Feb 6. Cleft Palate Craniofac J. 2016. PMID: 25658963 Review.
Evidence gathered in this review includes a variety of etiological factors that are causative or associated with both micrognathia and cleft palate. Observational studies relating the two abnormalities are also included. Much of the included literature recognizes a cause-a …
Evidence gathered in this review includes a variety of etiological factors that are causative or associated with both micrognathia an …
The ontogeny of Robin sequence.
Logjes RJH, Breugem CC, Van Haaften G, Paes EC, Sperber GH, van den Boogaard MH, Farlie PG. Logjes RJH, et al. Am J Med Genet A. 2018 Jun;176(6):1349-1368. doi: 10.1002/ajmg.a.38718. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696787 Review.
The triad of micrognathia, glossoptosis, and concomitant airway obstruction defined as "Robin sequence" (RS) is caused by oropharyngeal developmental events constrained by a reduced stomadeal space. ...
The triad of micrognathia, glossoptosis, and concomitant airway obstruction defined as "Robin sequence" (RS) is caused by oropharynge …
370 results