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Fetal and Pediatric Pathology Volume 33, 2014 - Issue 4

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CLINICOPATHOLOGIC CASE

Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing

Deepan MathurPediatric Pathology, Department of Pathology, and

Santhosh SomashekarDivision of Neonatology, Department of Pediatrics, University of Miami, Holtz Children's Hospital, Miami, Florida, USA

Cristina NavarreteDivision of Neonatology, Department of Pediatrics, University of Miami, Holtz Children's Hospital, Miami, Florida, USA

Maria M. RodriguezPediatric Pathology, Department of Pathology, andCorrespondence[email protected]

Pages 253-257 | Received 04 Mar 2014, Accepted 10 Mar 2014, Published online: 22 Apr 2014

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https://doi.org/10.3109/15513815.2014.904026
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Taizo A. Nakano, Alexander W. Rankin, Aparna Annam, Ann M. Kulungowski, Leslie M. McCallen, Lauren R. Hill & Kathryn C. Chatfield. (2022) Trametinib for Refractory Chylous Effusions and Systemic Complications in Children with Noonan Syndrome. The Journal of Pediatrics 248, pages 81-88.e1.
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Julia Sleutjes, Lotte Kleimeier, Erika Leenders, Willemijn Klein & Jos Draaisma. (2022) Lymphatic Abnormalities in Noonan Syndrome Spectrum Disorders: A Systematic Review. Molecular Syndromology 13:1, pages 1-11.
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Na Wang, Wen Shi & Yang Jiao. (2020) A PTPN11 mutation in a woman with Noonan syndrome and protein-losing enteropathy. BMC Gastroenterology 20:1.
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Leslie M. McCallen, Rebecca K. Ameduri, Susan W. Denfield, Debra A. Dodd, Melanie D. Everitt, Jonathan N. Johnson, Teresa M. Lee, Angela E. Lin, Jamie L. Lohr, Lindsay J. May, Mary Ella Pierpont, David A. Stevenson & Kathryn C. Chatfield. (2019) Cardiac transplantation in children with Noonan syndrome. Pediatric Transplantation 23:6.
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Kailyn Anderson, James Cnota, Jeanne James, Erin M. Miller, Ashley Parrott, Valentina Pilipenko, Kathryn Nicole Weaver & Amy Shikany. (2018) Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis. Congenital Heart Disease 14:2, pages 264-273.
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Pilar Carrasco Salas, Gertrudis Gómez-Molina, Páxedes Carreto-Alba, Reyes Granell-Escobar, Ignacio Vázquez-Rico & Antonio León-Justel. (2019) Noonan syndrome: Severe phenotype and PTPN11 mutations. Medicina Clínica 152:2, pages 62-64.
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Darius Ebrahimi-Fakhari, Eli Freiman, Monica H. Wojcik, Katie Krone, Alicia Casey, Ariel S. Winn, Amy E. Roberts & Beth D. Harper. (2017) Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome. The Journal of Pediatrics 185, pages 248-248.e1.
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Susan E. Wert. 2017. Fetal and Neonatal Physiology. Fetal and Neonatal Physiology 627 641.e3 .

Koichi OshimaHossein KhiabanianAna C. da Silva-AlmeidaGannie TzonevaFrancesco AbateAlberto Ambesi-ImpiombatoMarta Sanchez-MartinZachary CarpenterAlex PensonArianne Perez-GarciaCornelia EckertConcepción NicolasMilagros BalbinMaria Luisa SulisMotohiro KatoKatsuyoshi KohMaddalena PaganinGiuseppe BassoJulie M. Gastier-FosterMeenakshi DevidasMignon L. LohRenate Kirschner-SchwabeTeresa Palomero, Raul RabadanAdolfo A. Ferrando. (2016) Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia. Proceedings of the National Academy of Sciences 113:40, pages 11306-11311.
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Susan E. Wert & Kathryn A. Wikenheiser-Brokamp. 2016. Fetal and Neonatal Lung Development. Fetal and Neonatal Lung Development 94 125 .

Anne Slavotinek & Marwan Ali. (2015) Recognizable Syndromes in the Newborn Period. Clinics in Perinatology 42:2, pages 263-280.
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Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing

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Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing

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