Tendência familial das fissuras lábio-palatais

Souzafreitas, J. A.; Dalben, Gisele da Silva; Freitas, Patrícia; Santamaria, Milton

doi:10.1590/s1415-54192004000500009

Cited by 11 publications

(18 citation statements)

References 11 publications

(9 reference statements)

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“…CLP is one of the most common craniofacial malformations in mankind, being caused by failure in the union of facial processes in the embryonic period, resulting in a cleft that can extend from the lip to the soft palate, promoting changes in facial morphology, dentition, speech, esthetics, among others. [3] The available findings indicate that CLP affects about 1 in 700 live births. Furthermore, epidemiological and experimental data suggest that it presents a multifactorial origin.…”

Section: Literature Reviewmentioning

confidence: 99%

“…[1] Individuals with cleft lip and palate (CLP) can present lip irregularities even after several corrective surgeries, interfering with the esthetics and causing problems in self-esteem and social integration. [2][3][4] Thus, the aim of this study was to conduct a literature review regarding the possibility to use HA as a facial filler to correct the lip scar in individuals with CLP. The study comprised a literature review on the use of HA as a facial filler in the correction of lip scars from repair surgeries related to CLP, obtaining the necessary knowledge regarding the effectiveness of using HA as a facial filling material for these scars.…”

Section: Introductionmentioning

confidence: 99%

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The use of hyaluronic acid in individuals with cleft lip and palate: Literature review

Molena

Pinto

Dalben

2021

J Cleft Lip Palate Craniofac Anomal

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Since the Resolution 198/2019 of Brazilian Dental Council, which regulates orofacial harmonization as a dental specialty, and the advent of various uses of facial fillers, such as hyaluronic acid (HA), it is possible to perform both esthetic and functional corrections in individuals. Individuals with cleft lip and palate (CLP) present lip irregularities even after orofacial rehabilitation with an interdisciplinary team with several corrective surgeries, interfering with the esthetics, which can cause problems in self-esteem and social insertion. Thus, facial filling is an innovation that, together with dentistry, contributes to the individual's esthetics and well-being. Considering the patient safety and health, more research is progressively being conducted to make such procedures less invasive. This work conducted a literature review on the use of HA as a facial filler to correct lip scars in patients with CLP. By a literature and transverse search in Scientific Electronic Library Online and PubMed databases using specific descriptors, the studies that met the inclusion criteria were selected, from 1990 to 2020. It can be concluded that the use of HA as a facial filling material in the correction of lip scars from reparative surgeries related to CLP has been shown to be effective both for correction of facial asymmetry and to improve the quality of life of patients who used the procedure.

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Section: Literature Reviewmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

The use of hyaluronic acid in individuals with cleft lip and palate: Literature review

Molena

Pinto

Dalben

2021

J Cleft Lip Palate Craniofac Anomal

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“…Mas, por meio da identificação de genes responsáveis por síndromes envolvendo a FL/P, foi possível um maior entendimento também das FL/P não sindrômicas (BORGES et al, 2014; ALDHORAE et al, 2014). Alguns genes como o SATB2, TBX22 e o IRF6 entre outros, são considerados importantes no desenvolvimento do palato em humanos e têm sido associados à FP isolada por alguns grupos de pesquisadores (FITZPATRICK et al, 2003 apud MOSSEY et al, 2009; FU et al, 2015).Devido aos múltiplos aspectos descritos na etiologia das FL/P não sindrômicas, há extrema dificuldade em se identificar os fatores etiológicos específicos e da mesma forma em desenvolver programas preventivos confiáveis especialmente quanto à complexidade para se estabelecer um alvo de ação específico para a prevenção(SOUZA FREITAS et al, 2004). Dessa forma, a ampliação do conhecimento acerca da etiologia das FL/P permitiria melhorias no que se refere especialmente à prevenção(MOSSEY et al, 2009).…”

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Fissura de palato isolada não sindrômica: estudo do fenótipo, recorrência familial e histórico gestacional

Garbieri¹

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Dedico esta dissertação... A Deus, o grande responsável por todas as obras de minha vida, ao qual eu dedico além dessa dissertação toda minha vida e meu coração. Ao meu Amado Alexandre Keiti Miazaki, meu companheiro, que não mede esforços para ajudar no que for preciso em todos os momentos. Aos meus pais, Julineide e Luiz Antonio, ao meu irmão João Victor e a toda minha família. A todos que me acompanharam durante o período de realização deste trabalho. E a todos os pacientes do HRAC-USP. AGRADECIMENTOS Um eterno sentimento de gratidão tenho pela minha querida orientadora Dra. Lucimara Teixeira das Neves, quem eu admiro e confio tanto. Uma mãe científica, que me acolheu e me acompanha nesta jornada com muito carinho.

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“…Acometem cerca de 0,15% dos nascidos vivos e 5% dos filhos quando um genitor é afetado (SOUZA-FREITAS et al, 2004). Ocorrem entre o período embrionário e início do fetal.…”

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Estudo genético prospectivo de recém-nascidos e natimortos com defeitos congênitos

Oliveira¹

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Nós não devemos deixá-los de lado e pensarmos neles como algo inútil ou tratá-los como "curiosidades" ou "casualidades". Nenhum deles é desprovido de significado; e não há nenhum que não possa proporcionar um excelente conhecimento se apenas pudermos responder à questão: por que é raro? Ou, sendo raro, por que, neste caso, aconteceu? JAMES PAGET, Lancet, 2:1017, 1882 Aos meus pais, Maria Neusa e Florisvaldo Oliveira, pelo incentivo ao ensino e principalmente por todo carinho e atenção, ao meu irmão Vinicius Igor Oliveira e a todos meus familiares, por todo apoio.Aos meus amigos, pelo "suporte", obrigada! ResumoOs defeitos congênitos resultam de causas genéticas e não genéticas, afetam cerca de 3 a 5% dos recém-nascidos e são reconhecidos como uma das maiores causas de morbidade e mortalidade no primeiro ano de vida, além de serem a causa de muitas mortes embrionárias e fetais. Possuem etiologia e fatores de risco variados, muitos ainda desconhecidos. Dados AbstractBirth defects, resulting from genetic and non-genetic causes, affect about 3 to 5% of newborns and are recognized as a major cause of morbidity and mortality within the first year of life, as well as being the cause of many embryonic and fetal deaths. Not infrequently the varied etiology and risk factors remain unknown. Brazilian epidemiological data are scarce.The study of epidemiological factors may increase knowledge about these defects and make prevention strategies and genetic counseling possible for affected families. This work constitutes a prospective clinical genetic study of all newborn and stillborn infants with birth defects seen over one year in Hospital de Base in São José do Rio Preto, Sao Paulo, in order to estimate the prevalence, characterize the disease types, diagnoses or diagnostic categories and evaluate possible causes and consequences of the defects. Karyotypic analysis, a physical assessment, photographic records, an analysis of the patients' medical records and the collection of additional information with the family was performed for each infant. The study assessed 103 newborn and 7 stillborn subjects. The prevalence of birth defects was of 2.8%.A specific diagnosis was suggested in 82% of cases. Genetically-related birth defects were more prevalent than those with non-genetic etiology. Infants with multifactorial inheritance patterns were the most common (29%), followed by heterogeneous etiology (22%), monogenic inheritance patterns (19%), unknown (13,5%), chromosomal etiologies (12%) and environmental factors (4.5%). Maternal age, parental consanguinity and family susceptibility (the presence of defects in the family) were some of the identified risk factors. Most affected infants were premature and the most commonly observed consequences were prolonged hospital stays and death. Hence, birth defects are frequent in the population; several causes are involved with the genetic component being one of the most common, and the consequences can be severe. Knowledge of such defects makes the development of therapeutic and prevent...

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Tendência familial das fissuras lábio-palatais

Cited by 11 publications

References 11 publications

The use of hyaluronic acid in individuals with cleft lip and palate: Literature review

The use of hyaluronic acid in individuals with cleft lip and palate: Literature review

Fissura de palato isolada não sindrômica: estudo do fenótipo, recorrência familial e histórico gestacional

Estudo genético prospectivo de recém-nascidos e natimortos com defeitos congênitos

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