Literature DB >> 26803093

Noonan Syndrome Complicated by Primary Pulmonary Lymphangiectasia.

Jaclyn Jo Ford, Carol W Trotter.   

Abstract

Noonan syndrome is a genetic disorder that has several features common to other conditions, making diagnosis a challenge. This column summarizes the case of a neonate with an atypical presentation of Noonan syndrome involving a fatal type of lymphangiectasia resulting in persistent pleural effusions. Radiographic features of this condition are presented along with the complexities of diagnosis and treatment.

Entities:  

Mesh:

Year:  2015        PMID: 26803093     DOI: 10.1891/0730-0832.34.2.117

Source DB:  PubMed          Journal:  Neonatal Netw        ISSN: 0730-0832


  2 in total

Review 1.  Lymphatic Abnormalities in Noonan Syndrome Spectrum Disorders: A Systematic Review.

Authors:  Julia Sleutjes; Lotte Kleimeier; Erika Leenders; Willemijn Klein; Jos Draaisma
Journal:  Mol Syndromol       Date:  2021-09-10

Review 2.  Refractory thrombocytopenia could be a rare initial presentation of Noonan syndrome in newborn infants: a case report and literature review.

Authors:  Xiujun Tang; Zheng Chen; Xiaoxia Shen; Tian Xie; Xiaohong Wang; Taixiang Liu; Xiaolu Ma
Journal:  BMC Pediatr       Date:  2022-03-17       Impact factor: 2.125

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.