Noonan Syndrome Presenting as Lymphoedema Precox
DOI:
https://doi.org/10.3329/jom.v13i2.12771Keywords:
Noonan syndrome, LymphoedemaAbstract
Noonan Syndrome is an autosomal dominant disorder characterized by short stature, typical facial features and congenital heart defects. Other associated features are webbed neck, chest deformity, mild intellectual deficit, cryptorchidism, bleeding tendency and lymphatic dysplasia. We are reporting a 13 year old boy of Noonan syndrome presenting with lymphoedema of lower limb and genitalia.
DOI: http://dx.doi.org/10.3329/jom.v13i2.12771
J Medicine 2012; 13 : 243-245
Downloads
Download data is not yet available.
Abstract
111
111
PDF
90
90
Downloads
Published
2012-11-26
How to Cite
Haque, M. A., Sharmin, L. S., Amin, Z., & Ekram, A. S. (2012). Noonan Syndrome Presenting as Lymphoedema Precox. Journal of Medicine, 13(2), 243–245. https://doi.org/10.3329/jom.v13i2.12771
Issue
Section
Case Reports
License
Authors who publish with this journal agree to the following terms:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).
