Malformações detectadas pelo ultrassom abdominal em crianças com cardiopatia congênita

Malformações detectadas pelo ultrassom abdominal em crianças com cardiopatia congênita

FUNDAMENTO: Malformações extracardíacas podem estar presentes em pacientes com cardiopatia congênita (CC), trazendo maior risco de comorbidade e mortalidade. OBJETIVO: Verificar a frequência e os tipos de anormalidades abdominais detectadas em crianças com e sem CC através do ultrassom abdominal (US...

Full description

Bibliographic Details
Main Authors:	Rosana Cardoso Manique Rosa, Rafael Fabiano Machado Rosa, José Antônio Monteiro Flores, Eliete Golendziner, Ceres Andréia Vieira de Oliveira, Marileila Varella-Garcia, Giorgio Adriano Paskulin, Paulo Ricardo Gazzola Zen
Format:	Article
Language:	English
Published:	Sociedade Brasileira de Cardiologia (SBC)
Series:	Arquivos Brasileiros de Cardiologia
Subjects:	Ultrasonography Child Heart Defects, Congenital DiGeorge Syndrome Urogenital Abnormalities Chromosome Aberrations
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2012001500004&lng=en&tlng=en

Similar Items

Malformações detectadas pelo ultrassom abdominal em crianças com cardiopatia congênita Malformations detected by abdominal ultrasound in children with congenital heart disease
by: Rosana Cardoso Manique Rosa, et al.
Published: (2012-01-01)

Malformações detectadas pelo ultrassom abdominal em crianças com cardiopatia congênita Malformations detected by abdominal ultrasound in children with congenital heart disease
by: Rosana Cardoso Manique Rosa, et al.
Published: (2012-12-01)

Síndrome de deleção 22q11 e cardiopatias congênitas complexas 22q11.2 deletion syndrome and complex congenital heart defects
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-02-01)

Síndrome de deleção 22q11.2 e cardiopatias congênitas 22q11.2 deletion syndrome and congenital heart defects
by: Rafael Fabiano M. Rosa, et al.
Published: (2011-06-01)

Anterior laryngeal membrane and 22q11 deletion syndrome Membrana laríngea anterior e Síndrome de deleção 22q11
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-08-01)

Cardiopatias congênitas e malformações extracardíacas
by: Rosana Cardoso M. Rosa, et al.
Published: (2013-06-01)

Hematological abnormalities and 22q11.2 deletion syndrome
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-01-01)

Síndrome de deleção 22q11.2: importância da avaliação clínica e técnica de FISH 22q11.2 deletion syndrome: importance of clinical evaluation and FISH analysis
by: Dayane Bohn Koshiyama, et al.
Published: (2009-01-01)

Síndrome de deleção 22q11.2: compreendendo o CATCH22 22q11.2 deletion syndrome: catching the CATCH22
by: Rafael Fabiano M. Rosa, et al.
Published: (2009-06-01)

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance
by: Nicole E Spruijt, et al.
Published: (2014-07-01)

Features of Diagnosing and Managing a Patient with DiGeorge Syndrome
by: O.S. Koreniuk, et al.
Published: (2016-04-01)

Investigação de variações no número de cópias do DNA (Copy Number Variations, CNVs) em pacientes com suspeita clínica da Síndrome Velocardiofacial
by: Molck, Miriam Coelho, 1985-
Published: (2015)

Cardiac aspects of DiGeorge syndrome: a report of two cases with molecular analysis
by: Senka Mesihović Dinarević, et al.
Published: (2014-04-01)

DiGeorge syndrome who developed lymphoproliferative mediastinal mass
by: Kyu Yeun Kim, et al.
Published: (2015-03-01)

Disgenesias dentárias, alterações de tecido mole e morfologia craniofacial em pacientes com síndrome velocardiofacial e síndrome G/BBB
by: Gisele da Silva Dalben
Published: (2007)

Disgenesias dentárias, alterações de tecido mole e morfologia craniofacial em pacientes com síndrome velocardiofacial e síndrome G/BBB
by: Dalben, Gisele da Silva
Published: (2007)

Right Aortic Arch with a Retroesophageal Left Subclavian Artery and an Anomalous Origin of the Pulmonary Artery from the Aorta
by: Chang-Seok Jeon, et al.
Published: (2017-02-01)

Avaliação da função tímica em pacientes com Síndrome de DiGeorge
by: Angela Bueno Ferraz Fomin
Published: (2010)

Avaliação da função tímica em pacientes com Síndrome de DiGeorge
by: Fomin, Angela Bueno Ferraz
Published: (2010)

Evaluación citogenética y de pérdida de la heterocigosidad de la región 22q11.2 en pacientes con el Síndrome de DiGeorge = Cytogenetic evaluation and loss of heterozigocity of chromosome 22q11.2 in patients with the DiGeorge syndrome
by: Gallego García, Germán Andreo, et al.
Published: (2011-09-01)

Investigação laboratorial da síndrome velocardiofacial e possíveis fenocópias
by: Sgardioli, Ilária Cristina
Published: (2011)

Early-onset psychosis in an adolescent with DiGeorge syndrome: A case report
by: Keneilwe Molebatsi, et al.
Published: (2018-02-01)

High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups
by: A.C. Pereira, et al.
Published: (2003-10-01)

Clozapine-induced myocarditis in an adolescent male with DiGeorge Syndrome
by: Procaccini, D., et al.
Published: (2018)

Síndrome brânquio-óculo-facial (BOFS) e cardiopatias congênitas Síndrome branquio óculo facial (BOFS) y cardiopatías congénitas Branchio-oculo-facial syndrome (BOFS) and congenital heart defects
by: Rafael Fabiano Machado Rosa, et al.
Published: (2009-02-01)

Contribuições para o estabelecimento de estratégias laboratoriais em genética para a saúde pública no Brasil utilizando a síndrome de deleção 22q11.2 como modelo
by: Vieira, Tarsis Antonio Paiva, 1981-
Published: (2012)

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
by: Raad A. Haddad, et al.
Published: (2019-08-01)

Thymic Epithelium Abnormalities in DiGeorge and Down Syndrome Patients Contribute to Dysregulation in T Cell Development
by: Genni Enza Marcovecchio, et al.
Published: (2019-03-01)

Consideraciones anestésicas enpacientes con microdeleción del cromosoma 22q11
by: Ignacio Barra C., et al.
Published: (2019-03-01)

Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country
by: Amina Kurtovic-Kozaric, et al.
Published: (2016-03-01)

Follicular Helper T Cells in DiGeorge Syndrome
by: Adam Klocperk, et al.
Published: (2018-07-01)

Sail sign, significance in paediatrics and review of literature
by: Menon Narayanankutty Sunilkumar
Published: (2014-12-01)

Anormalidades cromossômicas entre pacientes com cardiopatia congênita
by: Patrícia Trevisan, et al.
Published: (2013-12-01)

Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells
by: Andrea Cirino, et al.
Published: (2020-09-01)

Optimisation de la différenciation neuronale et musculaire de cellules pluripotentes induites humaines pour la modélisation des maladies rares : exemple du syndrome de DiGeorge
by: Badja, Cherif
Published: (2015)

Verhaltensauffälligkeiten und elterliche Stressbelastung bei 22q11.2- Deletionssyndrom - eine Längsschnittstudie
by: Andritschky, Christoph
Published: (2013)

The Barriers and Quality of Care Issues for Individuals Diagnosed with 22q11.2 Deletion Syndrome
by: Miller, Barbara Bavette
Published: (2017)

Autoimmune hemolytic anemia associated with vitamin B12 deficiency and viral illness in DiGeorge syndrome. Case report and literature review
by: Zohaib Yousaf, et al.
Published: (2021-06-01)

Delayed diagnosis of annular pancreas in 11-year-old girl with DiGeorge syndrome
by: Mary Margaret Barr, et al.
Published: (2020-09-01)

Digeorge syndrome: A case report
by: Popović-Deušić Smiljka, et al.
Published: (2011-01-01)