Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Clin Genet ; 104(6): 713-715, 2023 12.
Artigo em Inglês | MEDLINE | ID: mdl-37612261

RESUMO

This study reports variants in BBS1 and BBS7 in patients with Bardet-Biedl syndrome from the Canadian Maritime provinces. The BBS1 variant NM_024649.5:c.1169T>G was identified as a recurrent variant in Prince Edward Island.


Assuntos
Síndrome de Bardet-Biedl , Proteínas Associadas aos Microtúbulos , Humanos , Canadá , Proteínas Associadas aos Microtúbulos/genética , Mutação , Ilha do Príncipe Eduardo
2.
Am J Med Genet A ; 191(2): 554-558, 2023 02.
Artigo em Inglês | MEDLINE | ID: mdl-36308391

RESUMO

Congenital heart defect (CHD) is a birth defect that affects the structure of the heart. Although CHD is often multifactorial, it can also be inherited as part of a Mendelian disorder such as in congenital heart defect and ectodermal dysplasia (CHDED). This disorder is caused by de novo variants in PRKD1. Here, we describe a patient with a novel de novo variant of PRKD1 with phenotypic features consistent with CHDED. Previously unreported features were noted including high intracranial pressure (ICP), partial anomalous pulmonary venous return (PAPVR), and bifid uvula. We suggest that these features may be associated with CHDED.


Assuntos
Fissura Palatina , Displasia Ectodérmica , Cardiopatias Congênitas , Humanos , Pressão Intracraniana , Cardiopatias Congênitas/complicações , Cardiopatias Congênitas/diagnóstico , Cardiopatias Congênitas/genética , Displasia Ectodérmica/complicações , Displasia Ectodérmica/diagnóstico , Displasia Ectodérmica/genética , Fenótipo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...