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Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA.
Nriagu, Bede N; Williams, Lydia S; Brewer, Niambi; Surrey, Lea F; Srinivasan, Abhay S; Li, Dong; Britt, Allison; Treat, James; Crowley, T Blaine; O'Connor, Nora; Ganguly, Arupa; Low, David; Queenan, Maria; Drivas, Theodore G; Zackai, Elaine H; Adams, Denise M; Hakonarson, Hakon; Snyder, Kristen M; Sheppard, Sarah E.
Afiliación
  • Nriagu BN; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Williams LS; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Brewer N; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Surrey LF; Genetic Diagnostic Laboratory, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Srinivasan AS; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Li D; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Britt A; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Treat J; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Crowley TB; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • O'Connor N; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Ganguly A; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Low D; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Queenan M; Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Drivas TG; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Zackai EH; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Adams DM; Genetic Diagnostic Laboratory, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Hakonarson H; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Snyder KM; Division of Plastic and Reconstructive Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Sheppard SE; Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Am J Med Genet A ; 194(1): 64-69, 2024 Jan.
Article en En | MEDLINE | ID: mdl-37705207
Turner syndrome (45,X) is caused by a complete or partial absence of a single X chromosome. Vascular malformations occur due to abnormal development of blood and/or lymphatic vessels. They arise from either somatic or germline pathogenic variants in the genes regulating growth and apoptosis of vascular channels. Aortic abnormalities are a common, known vascular anomaly of Turner syndrome. However, previous studies have described other vascular malformations as a rare feature of Turner syndrome and suggested that vascular abnormalities in individuals with Turner syndrome may be more generalized. In this study, we describe two individuals with co-occurrence of Turner syndrome and vascular malformations with a lymphatic component. In these individuals, genetic testing of the lesional tissue revealed a somatic pathogenic variant in PIK3CA-a known and common cause of lymphatic malformations. Based on this finding, we conclude that the vascular malformations presented here and likely those previously in the literature are not a rare part of the clinical spectrum of Turner syndrome, but rather a separate clinical entity that may or may not co-occur in individuals with Turner syndrome.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Turner / Anomalías Cardiovasculares / Anomalías Linfáticas / Malformaciones Vasculares Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Turner / Anomalías Cardiovasculares / Anomalías Linfáticas / Malformaciones Vasculares Límite: Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos