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Article

Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome.

The Journal of pediatrics - 1 Jun 2017

Ebrahimi-Fakhari Darius, Freiman Eli, Wojcik Monica H, Krone Katie, Casey Alicia, Winn Ariel S, Roberts Amy E, Harper Beth D

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Topics

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Share to PTPN11 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Noonan Syndrome

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

Source

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Identifiers

PMID: 28363362
DOI: 10.1016/j.jpeds.2017.02.042
PMCID: PMC5529256

Genes

PTPN11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome.PMID 28363362Read ↗

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Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome.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 ↗

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PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.Semantic proximity Read ↗

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