Database : MEDLINE
Search on : plagiocephaly [Words]
References found : 4509 [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

  2 / 4509 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

  3 / 4509 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

  4 / 4509 MEDLINE  
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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

  5 / 4509 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]: 29303454
[Au] Autor:Collett BR; Leroux BG; Wallace ER; Gallagher E; Shao J; Speltz ML
[Ad] Address:Departments of 1 Psychiatry and Behavioral Sciences.
[Ti] Title:Head shape at age 36 months among children with and without a history of positional skull deformation.
[So] Source:J Neurosurg Pediatr;21(3):204-213, 2018 Mar.
[Is] ISSN:1933-0715
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:OBJECTIVE In this study, the authors examined head shape through age 36 months for children with and without a history of positional plagiocephaly and/or brachycephaly (PPB). METHODS Infants with PPB (cases) were identified through a craniofacial clinic at the time of diagnosis. Infants without diagnosed PPB were identified through a participant registry. Clinician ratings of 3D cranial images were used to confirm the presence or absence of PPB. The cohort included 235 case infants (diagnosed PPB, confirmed with 3D imaging), 167 unaffected controls (no diagnosed PPB, no deformation detected), and 70 affected controls (no diagnosed PPB, discernible skull deformation). Participants were seen in infancy (age 7 months, on average) and again at ages 18 and 36 months. At each visit, automated 3D measures of skull deformation quantified posterior flattening and generated an absolute asymmetry score. The authors also used automated 2D measures to approximate overall asymmetry (approximate oblique cranial length ratio) and calculate the cephalic index. They used linear regression to compare cases to unaffected controls and to compare affected versus unaffected controls on all measures. They also calculated the proportion of children in each group with "persistent PPB," defined as one or more head shape measures above the 95th percentile relative to unaffected controls at 36 months. RESULTS Head shape became more rounded and symmetric for children with and without PPB, particularly between infancy and age 18 months. However, children with PPB continued to show greater skull deformation and asymmetry than unaffected controls at age 36 months. These differences were large in magnitude, ranging from 1 to 2 standard deviations (SDs), and in most (85.6%) of the cases, there was evidence of persistent PPB at 36 months. Similarly, although differences were more modest (i.e., 0.26-0.94 SD), affected controls continued to exhibit skull deformation on most measures relative to unaffected controls and approximately 30% had persistent PPB. Within the case group, head shape at 36 months was similar for untreated patients with PPB and for those who received helmet treatment and for patients with and without a history of torticollis. CONCLUSIONS Although head shape continues to improve, children with a history of skull deformation in infancy continue to exhibit measureable cranial flattening and asymmetry through age 36 months.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1801
[Cu] Class update date: 180304
[Lr] Last revision date:180304
[St] Status:In-Data-Review
[do] DOI:10.3171/2017.7.PEDS16693

  7 / 4509 MEDLINE  
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[PMID]: 29394478
[Au] Autor:Ditthakasem K; Kolar JC
[Ti] Title:Deformational Plagiocephaly: A Review.
[So] Source:Pediatr Nurs;43(2):59-64, 2017 Mar-Apr.
[Is] ISSN:0097-9805
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Deformational plagiocephaly (DP) is a common condition and the leading cause of head shape abnormalities in infants. It is characterized by asymmetrical distortion of the skull resulting from external forces on the back of the head. DP has become more prevalent in infants and has increased dramatically since the introduction in 1994 of the "Back to Sleep" campaign. Management of this condition is not often covered by insurance, and can be costly and lengthy; However, DP can be prevented. Early recognition and management can make a significant difference in patients' outcomes and reduce the cost of treatment. Nurses play a key role in recognition and prevention, are instrumental in educating parents and caregivers, and have a significant impact on preventing and reducing the risk of DP. Current systematic approaches to clinical assessment, diagnosis, and management strategies of DP can help nurses who care for infants and their families understand DP and take the necessary steps to prevent it.
[Mh] MeSH terms primary: Plagiocephaly, Nonsynostotic/nursing
[Mh] MeSH terms secundary: Humans
Infant
Plagiocephaly, Nonsynostotic/diagnosis
Plagiocephaly, Nonsynostotic/epidemiology
Plagiocephaly, Nonsynostotic/etiology
Prevalence
Risk Factors
Supine Position
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Em] Entry month:1803
[Cu] Class update date: 180301
[Lr] Last revision date:180301
[Js] Journal subset:N
[Da] Date of entry for processing:180203
[St] Status:MEDLINE

  8 / 4509 MEDLINE  
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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

  9 / 4509 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

  10 / 4509 MEDLINE  
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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


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