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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders

Fig. 1

Venny diagrams showing the existing overlaps among available gene lists in a diagnostic setting according to Orphanet, available to test patients with premature aging disorders (source: https://www.orpha.net/consor/cgi-bin/index.php) and data available on the laboratories’ websites (https://www.cegat.de/en/diagnostics/diagnostic-panels/connective-tissue-diseases/; http://www.chru-strasbourg.fr/sites/default/files/u110/NER_18genes_190308_2.pdf). We compare our gene panel with a panel of 55 genes asssociated with connective tissue diseases in Tübingen, Germany (CeGaT GmbH) and a panel of 18 genes associated with Cockayne and related syndromes, in Strasbourg, France (CHU de Strasbourg, Hôpital Civil)

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172