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Uniparental disomy of multiple chromosomes in two cases with a complex phenotype.
Polonis, Katarzyna; Lopes, Jaime L; Cabral, Huong; Babcock, Holly E; Kline, Laura; Ruiz, Kaylee M; Schwartz, Stuart; Hasadsri, Linda; Rowsey, Ross A; Hoppman, Nicole L.
Afiliación
  • Polonis K; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Lopes JL; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Cabral H; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Babcock HE; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Kline L; Rare Disease Institute, Children's National Hospital, Washington, DC, USA.
  • Ruiz KM; Women's Health and Genetics, Laboratory Corporation of America, Burlington, North Carolina, USA.
  • Schwartz S; Valley Children's Healthcare, Madera, California, USA.
  • Hasadsri L; Women's Health and Genetics, Laboratory Corporation of America, Burlington, North Carolina, USA.
  • Rowsey RA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Hoppman NL; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Am J Med Genet A ; 191(7): 1978-1983, 2023 07.
Article en En | MEDLINE | ID: mdl-37134191
Uniparental disomy (UPD) is the inheritance of both chromosomal homologs from one parent. Depending on the chromosome involved and the parental origin, UPD may result in phenotypic abnormalities due to aberrant methylation patterns or unmasking recessive conditions in isodisomic regions. UPD primarily originates from somatic rescue of a single meiotically-derived aneuploidy, most commonly a trisomy. Double UPD is exceedingly rare and triple UPD has not been previously described. Here, we report two unrelated clinical cases with UPD of multiple chromosomes; an 8-month-old male with maternal isodisomy of chromosome 7 and paternal isodisomy of chromosome 9, and a 4-week-old female with mixed paternal UPD for chromosomes 4, 10, and 14. These cases also demonstrate that although extremely rare, the detection of AOH on two or more chromosomes may warrant additional clinical and laboratory investigation such as methylation and STR marker analysis, especially when involving chromosomes known to be associated with imprinting disorders.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas / Disomía Uniparental Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas / Disomía Uniparental Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos