LymphedemaV1, Main, Exploration, bibRecord, 003A34

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

Identifieur interne : 003A34 ( Main/Exploration ); précédent : 003A33; suivant : 003A35

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

Auteurs : Fc Connell [Royaume-Uni] ; K. Gordon [Royaume-Uni] ; G. Brice [Royaume-Uni] ; V. Keeley [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; P. Ostergaard [Royaume-Uni]

Source :

Clinical Genetics [ 0009-9163 ] ; 2013-10.

RBID : ISTEX:5F2A7654CD7C9DAA3534AE59F2161DEBE4B4372A

Descripteurs français

KwdFr :
- Algorithmes, Humains, Lymphoedème (), Lymphoedème (diagnostic).
MESH :
- diagnostic : Lymphoedème.
- Algorithmes, Humains, Lymphoedème.

English descriptors

KwdEn :
- Algorithms, Humans, Lymphedema (classification), Lymphedema (diagnosis).
MESH :
- classification : Lymphedema.
- diagnosis : Lymphedema.
- Algorithms, Humans.

Abstract

Historically, primary lymphoedema was classified into just three categories depending on the age of onset of swelling; congenital, praecox and tarda. Developments in clinical phenotyping and identification of the genetic cause of some of these conditions have demonstrated that primary lymphoedema is highly heterogenous. In 2010, we introduced a new classification and diagnostic pathway as a clinical and research tool. This algorithm has been used to delineate specific primary lymphoedema phenotypes, facilitating the discovery of new causative genes. This article reviews the latest molecular findings and provides an updated version of the classification and diagnostic pathway based on this new knowledge.

Url:

https://api.istex.fr/document/5F2A7654CD7C9DAA3534AE59F2161DEBE4B4372A/fulltext/pdf

DOI: 10.1111/cge.12173

Affiliations:

Le document en format XML

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<front><div type="abstract">Historically, primary lymphoedema was classified into just three categories depending on the age of onset of swelling; congenital, praecox and tarda. Developments in clinical phenotyping and identification of the genetic cause of some of these conditions have demonstrated that primary lymphoedema is highly heterogenous. In 2010, we introduced a new classification and diagnostic pathway as a clinical and research tool. This algorithm has been used to delineate specific primary lymphoedema phenotypes, facilitating the discovery of new causative genes. This article reviews the latest molecular findings and provides an updated version of the classification and diagnostic pathway based on this new knowledge.</div>
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Serveur d'exploration sur le lymphœdème

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

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