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Transient neonatal diabetes mellitus in a child with invdup(6)(q22q23) of paternal origin.
Arthur, E I; Zlotogora, J; Lerer, I; Dagan, J; Marks, K; Abeliovich, D.
Afiliação
  • Arthur EI; Department of Neonatology, Shaare Zedek Medical Center, Jerusalem, Israel.
Eur J Hum Genet ; 5(6): 417-9, 1997.
Article em En | MEDLINE | ID: mdl-9450188
An association between the rare condition of transient neonatal diabetes mellitus and either uniparental disomy for chromosome 6 or dup(6)(q22q23) raised the assumption that in this location on chromosome 6 there is an imprinted gene. We diagnosed diabetes that developed in a baby girl immediately after birth and resolved after 7 weeks of insulin treatment. Due to some minor dysmorphic features, we investigated her karyotype and identified invdup(6)(q22q23). The duplication spans at least 10 cM including the DNA sites DS270,S314,S1684 and S310. This case further supports the assumption that an imprinted gene exists on chromosome 6q22-23.
Assuntos
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Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 6 / Aberrações Cromossômicas / Diabetes Mellitus Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 1997 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 6 / Aberrações Cromossômicas / Diabetes Mellitus Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 1997 Tipo de documento: Article