Literature DB >> 10912323

A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia.

S Oztürk1, K Cefle, S Palanduz, N B Erten, M A Karan, C Tasçioglu, S Umman, O Falay, S Vatansever, K Güler, S Cantez.   

Abstract

Noonan syndrome is characterised by a Turner-like phenotype and a normal karyotype. Although it is reported to be associated with abnormalities of the lymphatic system, involvement of the pulmonary lymphatics is rare. We present a case of Noonan syndrome where a whole body scintigraphy revealed lymphangiectasia of the lower extremities, abdomen and lungs.

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Year:  2000        PMID: 10912323

Source DB:  PubMed          Journal:  Int J Clin Pract        ISSN: 1368-5031            Impact factor:   2.503


  3 in total

1.  Noonan syndrome: clinical aspects and molecular pathogenesis.

Authors:  M Tartaglia; G Zampino; B D Gelb
Journal:  Mol Syndromol       Date:  2010-01-15

2.  Endothelial ERK signaling controls lymphatic fate specification.

Authors:  Yong Deng; Deepak Atri; Anne Eichmann; Michael Simons
Journal:  J Clin Invest       Date:  2013-02-08       Impact factor: 14.808

3.  A case of Noonan's syndrome with anomalous lymphorenal communication.

Authors:  Sanjeeva Goli; Vijay Kandimalla; Omar Khan
Journal:  JRSM Short Rep       Date:  2011-04-18
  3 in total

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