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2.
Pediatr Cardiol ; 38(7): 1519-1521, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28589408

RESUMO

This is a case report of premature low birth weight infant with hypoplasia of left heart structures and a large malaligned VSD who underwent successful staged approach of biventricular repair. We obtained qualitative and quantitative echocardiographic, MRI, and conventional catheterization data to support stepwise strategy towards LV rehabilitation to sustain adequate cardiac output. A thorough and intense follow-up has shown significant growth of left heart structures and favorable clinical status following staged biventricular repair. Our data indicate usefulness of qualitative and quantitative advanced complimentary multi-imaging modalities in predicting the postnatal growth potential of critically underdeveloped left heart structures.


Assuntos
Técnica de Fontan/métodos , Ventrículos do Coração/fisiopatologia , Síndrome do Coração Esquerdo Hipoplásico/fisiopatologia , Cateterismo Cardíaco/métodos , Ecocardiografia/métodos , Feminino , Ventrículos do Coração/diagnóstico por imagem , Humanos , Síndrome do Coração Esquerdo Hipoplásico/diagnóstico por imagem , Síndrome do Coração Esquerdo Hipoplásico/cirurgia , Lactente , Recém-Nascido de Baixo Peso , Recém-Nascido , Recém-Nascido Prematuro , Imagem Cinética por Ressonância Magnética/métodos , Estudos Retrospectivos
3.
Am J Med Genet ; 110(3): 273-7, 2002 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-12116237

RESUMO

We describe a 12-year-old boy with mosaic variegated aneuploidy (MVA), subnormal response to growth hormone (GH) stimulation testing, and short stature. In addition to features more commonly described in MVA such as microcephaly, cognitive deficits, and certain facial features, he also has features not commonly reported in MVA, including short limb segments, epidermoid cysts, ventricular septal defect, and subaortic stenosis. Chromosomal analysis revealed hyperdiploid chromosome numbers ranging from 47 to 70; modal number 50, in 24% of the metaphases. This case demonstrates that although the phenotype of MVA almost always includes growth failure, microcephaly, and mental retardation, additional features may vary greatly across individuals. His clinical features and course suggest that in addition to GH deficiency, he may have an intrinsic inability of the growth plate to respond to growth hormone.


Assuntos
Anormalidades Múltiplas/genética , Aneuploidia , Cardiopatias Congênitas/patologia , Hormônio do Crescimento Humano/deficiência , Anormalidades Múltiplas/patologia , Criança , Feminino , Transtornos do Crescimento/patologia , Humanos , Masculino , Microcefalia/patologia , Mosaicismo
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