Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 (H19/IGF2:TSS-DMR) in 11p15.5.
Clin Genet
; 98(4): 418-419, 2020 10.
Article
em En
| MEDLINE
| ID: mdl-33294970
ABSTRACT
The clinical impact of duplications affecting the 11p15.5 region is difficult to predict, and depends on the parent-of-origin of the affected allele as well as on the type (deletion, duplication), the extent and genomic content of the variant. Three unrelated families with inheritance of duplications affecting the IC1 region in 11p15.5 through two generations but different phenotypes (Beckwith-Wiedemann and Silver-Russell syndromes, normal phenotype) are reported. The inconsistent phenotypic patterns of carriers of the same variant strongly indicate the impact of cis- and/or trans-acting modifiers on the clinical outcome of IC1 duplication carriers.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Síndrome de Beckwith-Wiedemann
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Fator de Crescimento Insulin-Like II
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Predisposição Genética para Doença
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Síndrome de Silver-Russell
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RNA Longo não Codificante
Tipo de estudo:
Diagnostic_studies
/
Prognostic_studies
Limite:
Child
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Child, preschool
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Female
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Humans
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Infant
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Male
/
Newborn
Idioma:
En
Ano de publicação:
2020
Tipo de documento:
Article