Consensus recommendations on lymphedema in Phelan-McDermid syndrome

Author:

Damstra Robert J.ORCID,Vignes Stéphane,Mansour Sahar,Ravenswaaij-Arts Conny van

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference23 articles.

1. The Dutch lymphedema guidelines based on the international classification of functioning, disability, and health and the chronic care model;Damstra;J. Vasc. Surg.: Venous Lymph Dis,2017

2. 22q13.3 deletion syndrome: clinical and molecular analysis using array CGH;Dhar;Am. J. Med. Genet.,2010

3. The diagnosis and treatment of peripheral lymphedema: 2020 consensus document of the international society of Lymphology;Lymphology,2020

4. A novel mutation in CELSR1 is associated with hereditary lymphedema;Gonzalez-Garay;Vasc. Cell,2016

5. Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis;Gordon;J. Med. Genet.,2020

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