Database : MEDLINE
Search on : Craniosynostoses [Words]
References found : 4066 [refine]
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[PMID]: 29269540
[Ti] Title:Medivet to rethink breed policy after row.
[So] Source:Vet Rec;181(25):667, 2017 12 23.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Breeding/standards
Organizational Policy
Veterinary Medicine/organization & administration
[Mh] MeSH terms secundary: Animals
Craniosynostoses/prevention & control
Craniosynostoses/veterinary
Dog Diseases/prevention & control
Dogs
Humans
United Kingdom
[Pt] Publication type:NEWS
[Em] Entry month:1803
[Cu] Class update date: 180308
[Lr] Last revision date:180308
[Js] Journal subset:IM
[Da] Date of entry for processing:171223
[St] Status:MEDLINE

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[PMID]: 29269539
[Ti] Title:Welsh vets lead way with brachy position.
[So] Source:Vet Rec;181(25):666, 2017 12 23.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Breeding/standards
Craniosynostoses/veterinary
Dog Diseases/prevention & control
Organizational Policy
Veterinary Medicine/organization & administration
[Mh] MeSH terms secundary: Animals
Craniosynostoses/prevention & control
Dogs
Humans
Wales
[Pt] Publication type:NEWS
[Em] Entry month:1803
[Cu] Class update date: 180308
[Lr] Last revision date:180308
[Js] Journal subset:IM
[Da] Date of entry for processing:171223
[St] Status:MEDLINE

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[PMID]: 29246982
[Au] Autor:Waters A
[Ti] Title:At last! Action to stop brachy dogs ads.
[So] Source:Vet Rec;181(24):635, 2017 12 16.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Advertising as Topic
Craniosynostoses/veterinary
Dog Diseases/prevention & control
Periodicals as Topic
Veterinary Medicine
[Mh] MeSH terms secundary: Animal Welfare/standards
Animals
Breeding/standards
Craniosynostoses/prevention & control
Dogs
Humans
United Kingdom
[Pt] Publication type:EDITORIAL
[Em] Entry month:1803
[Cu] Class update date: 180307
[Lr] Last revision date:180307
[Js] Journal subset:IM
[Da] Date of entry for processing:171217
[St] Status:MEDLINE
[do] DOI:10.1136/vr.j5810

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[PMID]: 29246983
[Ti] Title:Enough is enough with brachy advertising.
[So] Source:Vet Rec;181(24):636-637, 2017 12 16.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Advertising as Topic
Craniosynostoses/veterinary
Dog Diseases/prevention & control
[Mh] MeSH terms secundary: Animal Welfare/standards
Animals
Breeding/standards
Craniosynostoses/prevention & control
Dogs
Humans
United Kingdom
[Pt] Publication type:NEWS
[Em] Entry month:1803
[Cu] Class update date: 180307
[Lr] Last revision date:180307
[Js] Journal subset:IM
[Da] Date of entry for processing:171217
[St] Status:MEDLINE

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[PMID]: 29280877
[Au] Autor:Lesciotto KM; Heuzé Y; Wang Jabs E; Bernstein JM; Richtsmeier JT
[Ad] Address:University Park, Pa.; New York, N.Y.; and Pessac, France From the Department of Anthropology, Pennsylvania State University; the Departments of Genetics and Genomic Sciences and Otolaryngology, Icahn School of Medicine at Mount Sinai; and the University of Bordeaux, Bordeaux Archaeological Sciences Cluster of Excellence.
[Ti] Title:Choanal Atresia and Craniosynostosis: Development and Disease.
[So] Source:Plast Reconstr Surg;141(1):156-168, 2018 01.
[Is] ISSN:1529-4242
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:A number of textbooks, review articles, and case reports highlight the potential comorbidity of choanal atresia in craniosynostosis patients. However, the lack of a precise definition of choanal atresia within the current craniosynostosis literature and widely varying methods of detection and diagnosis have produced uncertainty regarding the true coincidence of these conditions. The authors review the anatomy and embryologic basis of the human choanae, provide an overview of choanal atresia, and analyze the available literature that links choanal atresia and craniosynostosis. Review of over 50 case reports that describe patients diagnosed with both conditions reveals inconsistent descriptions of choanal atresia and limited use of definitive diagnostic methodologies. The authors further present preliminary analysis of three-dimensional medical head computed tomographic scans of children diagnosed with craniosynostosis syndromes (e.g., Apert, Pfeiffer, Muenke, and Crouzon) and typically developing children and, although finding no evidence of choanal atresia, report the potentially reduced nasal airway volumes in children diagnosed with Apert and Pfeiffer syndromes. A recent study of the Fgfr2c Crouzon/Pfeiffer syndrome mouse model similarly found a significant reduction in nasal airway volumes in littermates carrying this FGFR2 mutation relative to unaffected littermates, without detection of choanal atresia. The significant correlation between specific craniosynostosis syndromes and reduced nasal airway volume in mouse models for craniosynostosis and human pediatric patients indicates comorbidity of choanal and nasopharyngeal dysmorphologies and craniosynostosis conditions. Genetic, developmental, and epidemiologic sources of these interactions are areas particularly worthy of further research.
[Mh] MeSH terms primary: Abnormalities, Multiple
Choanal Atresia
Craniosynostoses
[Mh] MeSH terms secundary: Abnormalities, Multiple/diagnosis
Abnormalities, Multiple/embryology
Abnormalities, Multiple/genetics
Animals
Choanal Atresia/diagnosis
Choanal Atresia/embryology
Choanal Atresia/genetics
Craniosynostoses/diagnosis
Craniosynostoses/embryology
Craniosynostoses/genetics
Genetic Markers
Humans
Mice
Mutation
Nasopharynx/abnormalities
Nasopharynx/anatomy & histology
Nasopharynx/embryology
Receptor, Fibroblast Growth Factor, Type 2/genetics
Syndrome
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Nm] Name of substance:0 (Genetic Markers); EC 2.7.10.1 (FGFR2 protein, human); EC 2.7.10.1 (Fgfr2 protein, mouse); EC 2.7.10.1 (Receptor, Fibroblast Growth Factor, Type 2)
[Em] Entry month:1801
[Cu] Class update date: 180307
[Lr] Last revision date:180307
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:171228
[St] Status:MEDLINE
[do] DOI:10.1097/PRS.0000000000003928

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[PMID]: 29440606
[Au] Autor:Jeandel A; Garosi L
[Ad] Address:Davies Veterinary Specialists, Manor Farm Business Park, Higham Gobion, Herts, SG5 3HT, UK.
[Ti] Title:Gait abnormalities in brachycephalic breeds: should we be more concerned?
[So] Source:Vet Rec;182(6):164-166, 2018 02 10.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Breeding
Craniosynostoses
[Mh] MeSH terms secundary: Animals
Dog Diseases
Gait
[Pt] Publication type:JOURNAL ARTICLE; COMMENT
[Em] Entry month:1802
[Cu] Class update date: 180223
[Lr] Last revision date:180223
[Js] Journal subset:IM
[Da] Date of entry for processing:180215
[St] Status:MEDLINE
[do] DOI:10.1136/vr.k467

  7 / 4066 MEDLINE  
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[PMID]: 29374126
[Au] Autor:Evans M
[Ad] Address:PO Box 21, Cranleigh, Surrey GU6 7YB, UK.
[Ti] Title:Continuing the campaign on brachycephalic dogs.
[So] Source:Vet Rec;182(4):114, 2018 01 27.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Craniosynostoses/veterinary
Dog Diseases
[Mh] MeSH terms secundary: Airway Obstruction/veterinary
Animals
Dogs
[Pt] Publication type:LETTER; COMMENT
[Em] Entry month:1802
[Cu] Class update date: 180223
[Lr] Last revision date:180223
[Js] Journal subset:IM
[Da] Date of entry for processing:180128
[St] Status:MEDLINE
[do] DOI:10.1136/vr.k361

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[PMID]: 29384951
[Au] Autor:Ouyang L; Yang F
[Ad] Address:Department of Child Healthcare, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
[Ti] Title:Cole-Carpenter syndrome-1 with a de novo heterozygous deletion in the P4HB gene in a Chinese girl: A case report.
[So] Source:Medicine (Baltimore);96(52):e9504, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:RATIONALE: Cole-Carpenter syndrome-1 (CLCRP1) is an independent osteogenesis imperfect (OI)-like disorder that manifests as bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features. Only 2 types of mutation sites in the P4HB and CRTAP genes have been reported. PATIENT CONCERNS: A 14-month-old Chinese girl presented with prominent ocular proptosis, frontal bossing, craniosynostosis, plump anterior fontanel, growth retardation, osteopenia, and distinctive facial features that were strikingly similar to those in the original 2 cases. DIAGNOSES: Whole-exome sequencing revealed a novel deletion variation in exons 5 to 8 of the P4HB gene, which was found to be heterozygous using fluorogenic quantitative-polymerase chain reaction. LESSONS: This de novo deletion mutation in exons 5 to 8 of the P4HB gene advances our understanding of CLCRP1, expands the mutation spectrum of P4HB, and diversifies the cases reported for this condition.
[Mh] MeSH terms primary: Craniosynostoses/genetics
Eye Abnormalities/genetics
Hydrocephalus/genetics
Osteogenesis Imperfecta/genetics
Procollagen-Proline Dioxygenase/genetics
Protein Disulfide-Isomerases/genetics
[Mh] MeSH terms secundary: Asian Continental Ancestry Group
China
Craniosynostoses/pathology
Eye Abnormalities/pathology
Female
Humans
Hydrocephalus/pathology
Infant
Osteogenesis Imperfecta/pathology
Sequence Deletion
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Nm] Name of substance:EC 1.14.11.2 (Procollagen-Proline Dioxygenase); EC 5.3.4.1 (P4HB protein, human); EC 5.3.4.1 (Protein Disulfide-Isomerases)
[Em] Entry month:1802
[Cu] Class update date: 180220
[Lr] Last revision date:180220
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:180201
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009504

  9 / 4066 MEDLINE  
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[PMID]: 29438206
[Au] Autor:Koh KL; Zain A
[Ad] Address:Department of Plastic and Reconstructive Surgery, Hospital Kuala Lumpur, Jalan Pahang, Kuala Lumpur.
[Ti] Title:Surgical Outcome After Less "Rigid" Fixation in Open Cranial Vault Remodeling for Craniosynostosis.
[So] Source:J Craniofac Surg;, 2018 Feb 12.
[Is] ISSN:1536-3732
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:: Open cranial vault remodeling techniques require rigid fixation with hardware such as plates and screws; however, complications can occur. The purpose of this study was to assess the surgical outcome after open reconstruction for craniosynostosis with less rigid fixation using nonabsorbable suture. METHODS: Retrospective review of patients who underwent open craniofacial reconstruction for craniosynostosis at the Hospital Kuala Lumpur between January 2011 and December 2016 were performed. Demographic data, surgical complications, and postoperative aesthetic outcomes and reoperations were evaluated using Whitaker classification. Statistical analyses were performed using SPSS. RESULTS: Thirty-four (n = 34) cases were included in this review consisting of 16 males and 18 females (ratio 1:1.25). Sixteen patients were syndromic with multiple suture synostoses: Apert syndrome (n = 8), Crouzon syndrome (n = 6), and Muenke's syndrome (n = 2). Eighteen patients were nonsyndromic: isolated single-suture craniosynostosis (n = 12) and multiple suture involvement (n = 6). Mean age of presentation was 17.4 months (4-16 months) with mean age of surgery of 23.8 months (6-68 months). Mean length of surgery was 6.1 hours (range 3-10 hours) and mean length of hospital stay was 10 days (mean 7-20 days). Mean duration of follow-up was 2.2 years (6 month-4 years). There were a total of 9 complications postoperatively: massive blood loss (n = 4), seroma (n = 2), exposure keratitis (n = 1), hand extravasation (n = 1), and occipital sore (n = 1). Analysis showed multiple suture craniosynostoses were associated with longer operative times (4.3 hours vs 6.5 hours, P = 0.0082 < 0.05) and higher blood transfusion (170 mL vs 275 mL, P = 0.0274 < 0.05). Older age was also associated with higher blood transfusion (135.5 mL; <12 months vs 250.2 mL; 12-24 months vs 302.1 mL; >24 months of age, P = 0.00059). Patients were categorized as 88.2% (n = 30) Whitaker I and II and 11.8% (n = 4) Whitaker III and IV. Reoperation rates were 2.9% (n = 1). Whitaker III and IV class were higher among patients with syndromic synostosis, unicoronal and multiple suture synostoses. CONCLUSIONS: Our technique of open cranial reconstruction with nonabsorbable suture nylon 2/0 as sole method of fixation has resulted in good aesthetic outcome with low reoperations and complications rate. Longer follow-up is needed to ascertain our long-term results.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180213
[Lr] Last revision date:180213
[St] Status:Publisher
[do] DOI:10.1097/SCS.0000000000004347

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[PMID]: 28468154
[Au] Autor:Farber SJ; Nguyen DC; Skolnick GB; Naidoo SD; Smyth MD; Patel KB
[Ad] Address:*Division of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine †Department of Neurosurgery, Washington University School of Medicine, St Louis, MO.
[Ti] Title:Anthropometric Outcome Measures in Patients With Metopic Craniosynostosis.
[So] Source:J Craniofac Surg;28(3):713-716, 2017 May.
[Is] ISSN:1536-3732
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:PURPOSE: Treatment of metopic craniosynostosis is performed by either fronto-orbital advancement (FOA) or endoscopic-assisted techniques. Interfrontal angle (IFA) is a validated measure of trigonocephaly, but requires a computed tomography scan. The most common direct measure to assess surgical outcome in patients with trigonocephaly is frontal width (ft-ft). The aim of this study is to determine if frontal width correlates with IFA and successful surgical correction 1 year after treatment. A review of current morphologic assessment techniques is also provided. METHODS: Three-dimensional computed tomography scans (preoperative and 1 year postoperative) of patients who underwent FOA (n = 13) or endoscopic (n = 13) treatment of metopic craniosynostosis were reviewed. Age-matched scans of unaffected patients served as controls. Frontal width was measured by a straight line between the bilateral frontotemporal points. Measurements were performed by 2 experienced observers and compared to IFA. RESULTS: Mean frontal width at preoperative scan for endoscopic and open patients was 55 ±â€Š0.6 and 64 ±â€Š0.7 mm, respectively (Z-score 1.6 and -3.7). Mean frontal width at postoperative scan for endoscopic and open patients was 80 ±â€Š0.4 and 81 ±â€Š0.7 mm (Z-score 0.0 for both groups). Frontal width for endoscopic correction significantly correlated with IFA (r = 0.536, P = 0.005), as well as for the open patients (r = 0.704, P < 0.001). CONCLUSION: Frontal width normalizes 1 year after operation, regardless of technique. Advantage of frontal width is that it can be measured in the clinic using a spreading vernier caliper. It correlates well with IFA and can be used as a metric for morphologic outcome.
[Mh] MeSH terms primary: Anthropometry/methods
Craniosynostoses/diagnosis
Imaging, Three-Dimensional/methods
Tomography, X-Ray Computed/methods
[Mh] MeSH terms secundary: Craniosynostoses/surgery
Craniotomy/methods
Endoscopy/methods
Female
Humans
Infant
Male
Retrospective Studies
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180209
[Lr] Last revision date:180209
[Js] Journal subset:D
[Da] Date of entry for processing:170505
[St] Status:MEDLINE
[do] DOI:10.1097/SCS.0000000000003495


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