| Pierre Robin sequence: a series of 117 consecutive cases. | |
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MedLine Citation:
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PMID: 11598609 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A series of 117 cases of Pierre Robin Sequence are classified as isolated (48%), syndromic (35%), and with associated anomalies (17%); the latter group had a poor long-term prognosis. In isolated Pierre Robin Sequence, familial cases and a high incidence of twins were noted. Among syndromic Pierre Robin Sequence, 4 syndromes represent more than 50% of the diagnoses. |
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Authors:
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M Holder-Espinasse; V Abadie; V Cormier-Daire; C Beyler; Y Manach; A Munnich; S Lyonnet; G Couly; J Amiel |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: The Journal of pediatrics Volume: 139 ISSN: 0022-3476 ISO Abbreviation: J. Pediatr. Publication Date: 2001 Oct |
Date Detail:
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Created Date: 2001-10-12 Completed Date: 2001-12-04 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 0375410 Medline TA: J Pediatr Country: United States |
Other Details:
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Languages: eng Pagination: 588-90 Citation Subset: AIM; IM |
Affiliation:
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Department of Genetics, Necker Enfants-Malades Hospital, Paris, France. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Child, Preschool Female Genetic Counseling Humans Infant Infant, Newborn Longitudinal Studies Male Pedigree Pierre Robin Syndrome / diagnosis*, genetics*, mortality Prognosis Survival Rate |
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