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Article

Coronary artery dilatation in LEOPARD syndrome. A child case and literature review.

Congenital heart disease - 1 Jan 2000

Iwasaki Yoko, Horigome Hitoshi, Takahashi-Igari Miho, Kato Yoshiaki, Razzaque M Abdur, Matsuoka Rumiko

Abstract excerpt

LEOPARD syndrome (LS) is a rare inherited disease with multiple somatic abnormalities. LS and Noonan syndrome (NS) share many features, including cardiovascular disorders, and PTPN11 gene mutation is commonly reported in both syndromes. We report a 10-year-old male patient who was diagnosed as LS...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

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Source

Identifiers

PMID: 19207402
DOI: 10.1111/j.1747-0803.2008.00243.x

Genes

PTPN11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19207402-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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