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Noonan syndrome

Noonan syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_70356f18f09845a5895db925318ed4eb

Noonan syndrome

About this item

Full title

Noonan syndrome

Author / Creator

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2007-01, Vol.2 (1), p.4-4, Article 4

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital heart defects. The incidence of NS is estimated to be between 1:1000 and 1:2500 live births. The main facial features of NS are hypertelorism with down-slanting palpebral fissures, ptosis and low-set posteriorly rotated ears with a thickened helix. T...

Alternative Titles

Full title

Noonan syndrome

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_70356f18f09845a5895db925318ed4eb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_70356f18f09845a5895db925318ed4eb

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/1750-1172-2-4

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