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Article

Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Feb 2009

Sumi Muneichiro, Ohno Yasuharu, Sasaki Rie, Kondoh Tatsuro, Tagawa Masato, Masuzaki Hideaki, Moriuchi Hiroyuki

Abstract excerpt

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Topics

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Share to PTPN11 gene
Share to Infant, Newborn
Share to Mutation
Share to Noonan Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

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Source

Identifiers

PMID: 19371294
DOI: 10.1111/j.1442-200X.2008.02774.x

Genes

PTPN11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications.PMID 19371294Read ↗

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.Semantic proximity Read ↗

[Noonan's syndrome caused by a mutation in the PTPN11 gene].Semantic proximity Read ↗

Noonan syndrome: Severe phenotype and PTPN11 mutations.Semantic proximity Read ↗

Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome.Semantic proximity Read ↗

Noonan syndrome.Semantic proximity Read ↗

Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations.Semantic proximity Read ↗

Refractory thrombocytopenia could be a rare initial presentation of Noonan syndrome in newborn infants: a case report and literature review.Semantic proximity Read ↗

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment.Semantic proximity Read ↗

Early fetal death associated with compound heterozygosity for Noonan syndrome-causative PTPN11 mutations.Semantic proximity Read ↗

Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation.Semantic proximity Read ↗

Does the rare A172G mutation of PTPN11 gene convey a mild Noonan syndrome phenotype?Semantic proximity Read ↗

[Noonan syndrome and Leopard syndrome linked to mutation of the gene PTPN11].Semantic proximity Read ↗

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