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[PMID]:28369379
[Au] Autor:Kim S; Twigg SRF; Scanlon VA; Chandra A; Hansen TJ; Alsubait A; Fenwick AL; McGowan SJ; Lord H; Lester T; Sweeney E; Weber A; Cox H; Wilkie AOM; Golden A; Corsi AK
[Ad] Endereço:Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
[Ti] Título:Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans.
[So] Source:Hum Mol Genet;26(11):2118-2132, 2017 Jun 01.
[Is] ISSN:1460-2083
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Twist transcription factors, members of the basic helix-loop-helix family, play crucial roles in mesoderm development in all animals. Humans have two paralogous genes, TWIST1 and TWIST2, and mutations in each gene have been identified in specific craniofacial disorders. Here, we describe a new clinical entity, Sweeney-Cox syndrome, associated with distinct de novo amino acid substitutions (p.Glu117Val and p.Glu117Gly) at a highly conserved glutamic acid residue located in the basic DNA binding domain of TWIST1, in two subjects with frontonasal dysplasia and additional malformations. Although about one hundred different TWIST1 mutations have been reported in patients with the dominant haploinsufficiency Saethre-Chotzen syndrome (typically associated with craniosynostosis), substitutions uniquely affecting the Glu117 codon were not observed previously. Recently, subjects with Barber-Say and Ablepharon-Macrostomia syndromes were found to harbor heterozygous missense substitutions in the paralogous glutamic acid residue in TWIST2 (p.Glu75Ala, p.Glu75Gln and p.Glu75Lys). To study systematically the effects of these substitutions in individual cells of the developing mesoderm, we engineered all five disease-associated alleles into the equivalent Glu29 residue encoded by hlh-8, the single Twist homolog present in Caenorhabditis elegans. This allelic series revealed that different substitutions exhibit graded severity, in terms of both gene expression and cellular phenotype, which we incorporate into a model explaining the various human disease phenotypes. The genetic analysis favors a predominantly dominant-negative mechanism for the action of amino acid substitutions at this highly conserved glutamic acid residue and illustrates the value of systematic mutagenesis of C. elegans for focused investigation of human disease processes.
[Mh] Termos MeSH primário: Proteínas Nucleares/metabolismo
Proteínas Repressoras/metabolismo
Proteína 1 Relacionada a Twist/metabolismo
[Mh] Termos MeSH secundário: Anormalidades Múltiplas
Acrocefalossindactilia
Sequência de Aminoácidos
Substituição de Aminoácidos
Animais
Sequência de Bases/genética
Caenorhabditis elegans/genética
Caenorhabditis elegans/metabolismo
Criança
Pré-Escolar
Modelos Animais de Doenças
Anormalidades do Olho
Haploinsuficiência
Sequências Hélice-Alça-Hélice
Seres Humanos
Macrostomia
Masculino
Mutação
Proteínas Nucleares/genética
Fenótipo
Domínios Proteicos/genética
Proteínas Repressoras/genética
Fatores de Transcrição/genética
Proteína 1 Relacionada a Twist/genética
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Nuclear Proteins); 0 (Repressor Proteins); 0 (TWIST1 protein, human); 0 (TWIST2 protein, human); 0 (Transcription Factors); 0 (Twist-Related Protein 1)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171017
[Lr] Data última revisão:
171017
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170404
[St] Status:MEDLINE
[do] DOI:10.1093/hmg/ddx107


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[PMID]:27793865
[Au] Autor:Simonse E; Panis B; Busari JO
[Ad] Endereço:Zuyderland Medisch Centrum, Heerlen, The Netherlands.
[Ti] Título:Unilateral macrostomia in the newborn: a rare congenital anomaly of the oral commissure.
[So] Source:BMJ Case Rep;2016, 2016 Oct 28.
[Is] ISSN:1757-790X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Macrostomia is a rare medical condition, defined as an enlargement of the mouth at the oral commissure. The incidence varies between 1 in 60 000 to 1 in 300 000 live births. Macrostomia is a form of a facial cleft. Macrostomia can present as a unilateral or bilateral anomaly with a partial or complete cleft. Associated anomalies of the surrounding bone, muscle and soft tissue can also be present with or without the presence of a syndrome. Macrostomia results in aesthetic disharmony and also in functional problems. In both cases surgery is the treatment of choice. In cases of macrostomia, additional investigations should be performed to rule out accompanying cardiac and renal anomalies and associated syndromes. A multidisciplinary approach and good collaboration between healthcare providers is essential for optimal care of these patients.
[Mh] Termos MeSH primário: Fenda Labial/diagnóstico
Pavilhão Auricular/anormalidades
Macrostomia/diagnóstico
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/diagnóstico
Seres Humanos
Recém-Nascido
Masculino
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170306
[Lr] Data última revisão:
170306
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161030
[St] Status:MEDLINE


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[PMID]:27196381
[Au] Autor:De Maria B; Mazzanti L; Roche N; Hennekam RC
[Ad] Endereço:Department of Pediatrics and Translational Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
[Ti] Título:Barber-Say syndrome and Ablepharon-Macrostomia syndrome: An overview.
[So] Source:Am J Med Genet A;170(8):1989-2001, 2016 Aug.
[Is] ISSN:1552-4833
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Barber-Say syndrome (BSS) and Ablepharon-Macrostomia syndrome (AMS) are congenital malformation syndromes caused by heterozygous mutations in TWIST2. Here we provide a critical review of all patients published with these syndromes. We excluded several earlier reports due to misdiagnosis or insufficient data for reliable confirmation of the diagnosis. There remain 16 reliably diagnosed individuals with BSS and 16 with AMS. Major facial characteristics present in both entities, albeit often in differing frequencies, are excessive facial creases, hypertelorism, underdevelopment of the anterior part of the eyelids (anterior lamella), ectropion, broad nasal ridge and tip, thick and flaring alae nasi, protruding maxilla, wide mouth, thin upper vermillion, and attached ear lobes. In BSS a remarkable extension of the columella on the philtrum can be seen, and in both the medial parts of the cheeks bulge towards the corners of the mouth (cheek pads). Scalp hair is sparse in AMS only, but sparse eyebrows and eyelashes occur in both entities, and general hypertrichosis occurs in BSS. We compare these characteristics with those in Setleis syndrome which can also be caused by TWIST2 mutations. The resemblance between the three syndromes is considerable, and likely differences seem larger than they actually are due to insufficiently complete evaluation for all characteristics of the three entities in the past. It is likely that with time it can be concluded that BSS. AMS and Setleis syndrome form a continuum. © 2016 Wiley Periodicals, Inc.
[Mh] Termos MeSH primário: Anormalidades Múltiplas/diagnóstico
Anormalidades do Olho/diagnóstico
Doenças Palpebrais/diagnóstico
Hirsutismo/diagnóstico
Hipertelorismo/diagnóstico
Hipertricose/diagnóstico
Macrostomia/diagnóstico
Fenótipo
Anormalidades da Pele/diagnóstico
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/genética
Anormalidades do Olho/genética
Doenças Palpebrais/genética
Facies
Estudos de Associação Genética
Genótipo
Hirsutismo/genética
Seres Humanos
Hipertelorismo/genética
Hipertricose/genética
Macrostomia/genética
Mutação
Anormalidades da Pele/genética
Proteína 2 Relacionada a Twist/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; REVIEW
[Nm] Nome de substância:
0 (Twist-Related Protein 2)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171024
[Lr] Data última revisão:
171024
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160520
[St] Status:MEDLINE
[do] DOI:10.1002/ajmg.a.37757


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[PMID]:27092433
[Au] Autor:Singh A; Schanze D; Agarwal N; Prasad R; Mishra OP; Singh R; Kapoor S; Zenker M
[Ad] Endereço:aGenetic and Metabolic Clinic, Department of Pediatrics Departments of bPediatrics cAnatomy, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh dDivision of Genetics, Department of Pediatrics, MAMC Associated Lok Nayak Hospital, New Delhi, India eInstitute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
[Ti] Título:Transmission of Barber-Say syndrome from a mosaic father to his child in an Indian family.
[So] Source:Clin Dysmorphol;25(4):181-5, 2016 Oct.
[Is] ISSN:1473-5717
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Doenças Palpebrais/diagnóstico
Doenças Palpebrais/genética
Hirsutismo/diagnóstico
Hirsutismo/genética
Hipertelorismo/diagnóstico
Hipertelorismo/genética
Hipertricose/diagnóstico
Hipertricose/genética
Macrostomia/diagnóstico
Macrostomia/genética
Mosaicismo
Herança Paterna
Anormalidades da Pele/diagnóstico
Anormalidades da Pele/genética
[Mh] Termos MeSH secundário: Adulto
Análise Mutacional de DNA
Facies
Feminino
Seres Humanos
Índia
Lactente
Masculino
Mutação
Linhagem
Fenótipo
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170206
[Lr] Data última revisão:
170206
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160420
[St] Status:MEDLINE
[do] DOI:10.1097/MCD.0000000000000127


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[PMID]:26703052
[Au] Autor:Kobraei EM; Lentz AK; Eberlin KR; Hachach-Haram N; Hamdan US
[Ad] Endereço:*Division of Plastic and Reconstructive Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA †Division of Plastic and Reconstructive Surgery, University of Florida Health Science Center, University of Florida College of Medicine, Gainesville, FL ‡Department of Plastic Surgery, Guy's & St. Thomas' Hospital, London, United Kingdom §Global Smile Foundation, Tufts University School of Medicine, Harvard Medical School, and Clinical Instructor of Otolaryngology, Boston University School of Medicine. Boston, MA.
[Ti] Título:Macrostomia: A Practical Guide for Plastic and Reconstructive Surgeons.
[So] Source:J Craniofac Surg;27(1):118-23, 2016 Jan.
[Is] ISSN:1536-3732
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Macrostomia is a rare and debilitating congenital anomaly with incompletely understood etiopathogenesis. Despite the phenotypic variability in macrostomia, plastic surgeons should demonstrate competence in the diagnosis and management of this condition. The anatomy, embryology, classification, and clinical presentation of macrostomia are reviewed in this manuscript. A historical overview of surgical repair is presented that forms the basis for understanding modern techniques of repair. Finally, an effective method of macrostomia repair is presented along with review of 5-year results. It is our intent that this guide serve as a reference for plastic and reconstructive surgeons to accomplish safe, functional, and aesthetic macrostomia reconstruction.
[Mh] Termos MeSH primário: Macrostomia/cirurgia
Procedimentos Cirúrgicos Reconstrutivos/métodos
[Mh] Termos MeSH secundário: Pontos de Referência Anatômicos/patologia
Cicatriz/etiologia
Deformidades Dentofaciais/diagnóstico
Deformidades Dentofaciais/cirurgia
Procedimentos Cirúrgicos Dermatológicos/métodos
Músculos Faciais/cirurgia
Feminino
Seres Humanos
Lactente
Lábio/cirurgia
Macrostomia/diagnóstico
Mucosa Bucal/cirurgia
Complicações Pós-Operatórias
Cuidados Pré-Operatórios
Retalhos Cirúrgicos/cirurgia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1609
[Cu] Atualização por classe:160109
[Lr] Data última revisão:
160109
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:151226
[St] Status:MEDLINE
[do] DOI:10.1097/SCS.0000000000002294


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[PMID]:26267577
[Au] Autor:Tuin J; Tahiri Y; Paliga JT; Taylor JA; Bartlett SP
[Ad] Endereço:*Division of Plastic Surgery, Children's Hospital of Philadelphia, The Perelman School of Medicine at the University of Pennsylvania, PA †Division of Plastic Surgery, Riley Hospital for Children, Indiana University, IN.
[Ti] Título:Distinguishing Goldenhar Syndrome from Craniofacial Microsomia.
[So] Source:J Craniofac Surg;26(6):1887-92, 2015 Sep.
[Is] ISSN:1536-3732
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Goldenhar syndrome is characterized by the typical features of craniofacial microsomia (CFM) with the addition of epibulbar dermoids and vertebral anomalies. The aim of this study is to examine the objective differences between patients carrying a diagnosis of Goldenhar syndrome to those diagnosed with CFM. Thus, we performed an Institutional Review Board-approved retrospective chart review on all patients who presented with a diagnosis of CFM or Goldenhar syndrome from January 1990 to December 2012. Demographic, diagnosis, OMENS+ classification, accompanying diagnoses, and radiographic data were collected. For subjective analysis, subgroups were designed based on the diagnosis Goldenhar syndrome or CFM per history. For objective analysis, subgroups were designed based on the presence of epibulbar dermoids and/or vertebral anomalies. The cohorts were compared with respect to associated medical abnormalities and severity of CFM features. One hundred thirty eight patients met inclusion criteria. Epibulbar dermoids and vertebral anomalies were seen in 17% and 34% of the patients, respectively. Only 10 patients (7.2%) had both epibulbar dermoids and vertebral anomalies. The subjective "Goldenhar" group (N = 44, 32%) was found to have a higher percentage of bilaterally affected patients (P = 0.001), a more severe mandibular deformity (P = <0.001), a more severe soft tissue deformity (P = 0.01), and a higher incidence of macrostomia (P = 0.003). In the objective subgroup analysis, the only significant difference was found in the degree of soft tissue deficiency (P = 0.049). The diagnostic criteria of Goldenhar syndrome remain unclear, thereby making clinical use of the term "Goldenhar" inconsequential. Goldenhar syndrome is over diagnosed subjectively in patients who show more severe CFM features.
[Mh] Termos MeSH primário: Síndrome de Goldenhar/diagnóstico
[Mh] Termos MeSH secundário: Criança
Estudos de Coortes
Anormalidades Craniofaciais/diagnóstico
Cisto Dermoide/diagnóstico
Diagnóstico Diferencial
Orelha Externa/anormalidades
Neoplasias Palpebrais/diagnóstico
Doenças do Nervo Facial/diagnóstico
Feminino
Cardiopatias Congênitas/diagnóstico
Seres Humanos
Imagem Tridimensional/métodos
Rim/anormalidades
Macrostomia/diagnóstico
Masculino
Mandíbula/anormalidades
Órbita/anormalidades
Estudos Retrospectivos
Coluna Vertebral/anormalidades
Tomografia Computadorizada por Raios X/métodos
Traqueostomia/estatística & dados numéricos
[Pt] Tipo de publicação:COMPARATIVE STUDY; JOURNAL ARTICLE
[Em] Mês de entrada:1603
[Cu] Atualização por classe:150911
[Lr] Data última revisão:
150911
[Sb] Subgrupo de revista:D
[Da] Data de entrada para processamento:150813
[St] Status:MEDLINE
[do] DOI:10.1097/SCS.0000000000002017


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[PMID]:26119818
[Au] Autor:Marchegiani S; Davis T; Tessadori F; van Haaften G; Brancati F; Hoischen A; Huang H; Valkanas E; Pusey B; Schanze D; Venselaar H; Vulto-van Silfhout AT; Wolfe LA; Tifft CJ; Zerfas PM; Zambruno G; Kariminejad A; Sabbagh-Kermani F; Lee J; Tsokos MG; Lee CC; Ferraz V; da Silva EM; Stevens CA; Roche N; Bartsch O; Farndon P; Bermejo-Sanchez E; Brooks BP; Maduro V; Dallapiccola B; Ramos FJ; Chung HY; Le Caignec C; Martins F; Jacyk WK; Mazzanti L; Brunner HG; Bakkers J; Lin S; Malicdan MC; Boerkoel CF; Gahl WA; de Vries BB; van Haelst MM; Zenker M; Markello TC
[Ad] Endereço:NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA; Department of Pediatrics, Walter Reed National Military Medical Center, Bethesda, MD 20892, USA.
[Ti] Título:Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.
[So] Source:Am J Hum Genet;97(1):99-110, 2015 Jul 02.
[Is] ISSN:1537-6605
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Ablepharon macrostomia syndrome (AMS) and Barber-Say syndrome (BSS) are rare congenital ectodermal dysplasias characterized by similar clinical features. To establish the genetic basis of AMS and BSS, we performed extensive clinical phenotyping, whole exome and candidate gene sequencing, and functional validations. We identified a recurrent de novo mutation in TWIST2 in seven independent AMS-affected families, as well as another recurrent de novo mutation affecting the same amino acid in ten independent BSS-affected families. Moreover, a genotype-phenotype correlation was observed, because the two syndromes differed based solely upon the nature of the substituting amino acid: a lysine at TWIST2 residue 75 resulted in AMS, whereas a glutamine or alanine yielded BSS. TWIST2 encodes a basic helix-loop-helix transcription factor that regulates the development of mesenchymal tissues. All identified mutations fell in the basic domain of TWIST2 and altered the DNA-binding pattern of Flag-TWIST2 in HeLa cells. Comparison of wild-type and mutant TWIST2 expressed in zebrafish identified abnormal developmental phenotypes and widespread transcriptome changes. Our results suggest that autosomal-dominant TWIST2 mutations cause AMS or BSS by inducing protean effects on the transcription factor's DNA binding.
[Mh] Termos MeSH primário: Anormalidades Múltiplas/genética
Anormalidades do Olho/genética
Doenças Palpebrais/genética
Hirsutismo/genética
Hipertelorismo/genética
Hipertricose/genética
Macrostomia/genética
Modelos Moleculares
Fenótipo
Proteínas Repressoras/genética
Anormalidades da Pele/genética
Proteína 1 Relacionada a Twist/genética
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/patologia
Sequência de Aminoácidos
Animais
Sequência de Bases
Imunoprecipitação da Cromatina
Exoma/genética
Anormalidades do Olho/patologia
Doenças Palpebrais/patologia
Células HeLa
Hirsutismo/patologia
Seres Humanos
Hipertelorismo/patologia
Hipertricose/patologia
Macrostomia/patologia
Microscopia Eletrônica
Dados de Sequência Molecular
Mutação de Sentido Incorreto/genética
Conformação Proteica
Proteínas Repressoras/química
Análise de Sequência de DNA
Anormalidades da Pele/patologia
Proteína 1 Relacionada a Twist/química
Peixe-Zebra
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Repressor Proteins); 0 (TWIST2 protein, human); 0 (Twist-Related Protein 1)
[Em] Mês de entrada:1509
[Cu] Atualização por classe:161125
[Lr] Data última revisão:
161125
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150630
[St] Status:MEDLINE


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[PMID]:25245233
[Au] Autor:Bayram M; Yildirim M; Seymen F
[Ad] Endereço:Department of Pedodontics, School of Dentistry, Istanbul Medipol University, 34083, Istanbul, Turkey, dentistmerve@gmail.com.
[Ti] Título:Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome.
[So] Source:Eur Arch Paediatr Dent;16(1):63-6, 2015 Feb.
[Is] ISSN:1818-6300
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: The Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth condition characterised by macrosomia, mental deficiency, large head, prominent skull sutures, midface deficiency, hypertelorism, broad nose, wide mouth, macroglossia, malocclusion, highly arched palate, and musculoskeletal and limb abnormalities. The aim of this case report is to present clinical and oral findings of an 8-year-old boy who had been diagnosed with SGBS. CASE REPORT: This patient had supernumerary nipples on the right side, cubitus valgus webbed fingers, scoliosis, umbilical hernia, a coarse face, macrocephaly, hypertelorism, a short broad nose, a wide mouth, a straight facial profile and hearing loss. The patient also had macroglossia, diastemas, over-retained primary tooth, absent mandibular permanent central incisors, and highly arched palate. Lateral cephalometric analysis revealed a large anterior cranial base, a large maxilla and mandible, a large inferior face height, and skeletal Class III jaw relationship. FOLLOW-UP: After extraction of the over-retained primary central tooth, a partial prosthesis was fabricated in order to maintain function. The patient has been recalled regularly at 6-month intervals for 2 years. Over the following years the prosthesis was replaced due to facial growth. CONCLUSION: Long term follow-up is essential for the patient with SGBS. Preventive dental care, including oral hygiene instructions, diet counselling and the use of fluoride has been implemented.
[Mh] Termos MeSH primário: Anodontia/diagnóstico
Arritmias Cardíacas/diagnóstico
Doenças Genéticas Ligadas ao Cromossomo X/diagnóstico
Gigantismo/diagnóstico
Cardiopatias Congênitas/diagnóstico
Deficiência Intelectual/diagnóstico
Macroglossia/diagnóstico
Má Oclusão de Angle Classe III/diagnóstico
[Mh] Termos MeSH secundário: Cefalometria/métodos
Criança
Prótese Parcial Removível
Diastema/patologia
Seguimentos
Seres Humanos
Hipertelorismo/diagnóstico
Incisivo/anormalidades
Macrostomia/diagnóstico
Masculino
Nariz/anormalidades
Palato/anormalidades
Dente Decíduo/patologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1601
[Cu] Atualização por classe:171114
[Lr] Data última revisão:
171114
[Sb] Subgrupo de revista:D; IM
[Da] Data de entrada para processamento:140924
[St] Status:MEDLINE
[do] DOI:10.1007/s40368-014-0141-0


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[PMID]:25665332
[Au] Autor:Gleizal A; Bourlet J; Saint Amand J; Zulma C; Bachelet JT
[Ti] Título:[Oro-dental development and anomalies].
[Ti] Título:Développement buccodentaire et anomalies..
[So] Source:Rev Prat;64(10):1445-56, 2014 Dec.
[Is] ISSN:0035-2640
[Cp] País de publicação:France
[La] Idioma:fre
[Mh] Termos MeSH primário: Anormalidades da Boca/diagnóstico
Boca/embriologia
Anormalidades Dentárias/diagnóstico
Erupção Ectópica de Dente/diagnóstico
[Mh] Termos MeSH secundário: Anodontia
Fenda Labial
Fissura Palatina
Anormalidades Craniofaciais/diagnóstico
Hipoplasia do Esmalte Dentário
Educação Médica Continuada
Paralisia Facial/diagnóstico
Dentes Fusionados
Seres Humanos
Macroglossia
Macrostomia
Má Oclusão/diagnóstico
Glândulas Salivares/anormalidades
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1504
[Cu] Atualização por classe:150210
[Lr] Data última revisão:
150210
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150211
[St] Status:MEDLINE


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[PMID]:25069316
[Au] Autor:Li YH; Ge RL
[Ti] Título:[Correlation research between changes of breathing during sleep and AMS].
[So] Source:Sheng Li Ke Xue Jin Zhan;45(2):154-8, 2014 Apr.
[Is] ISSN:0559-7765
[Cp] País de publicação:China
[La] Idioma:chi
[Mh] Termos MeSH primário: Anormalidades Múltiplas
Anormalidades do Olho
Macrostomia
Respiração
Sono
[Mh] Termos MeSH secundário: Seres Humanos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1606
[Cu] Atualização por classe:140729
[Lr] Data última revisão:
140729
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:140730
[St] Status:MEDLINE



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BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde