Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Pulmonary surfactant protein gene mutation associated with pediatric interstitial lung disease: a case study and the review of related literature].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Feb 2013

Zhu Chun-mei, Cao Ling, Huang Rong-yan, Wang Ya-jun, Zou Ji-zhen, Yuan Xin-yu, Song Fang, Chen Hui-zhong

Abstract excerpt

OBJECTIVE: To report a case of pulmonary surfactant protein (SP) gene mutation associated with pediatric interstitial lung disease, and study the clinical diagnosis process and review of related literature, to understand the relationship between interstitial lung disease and SP gene mutation in infants and children. METHOD: The clinical, radiological, histological, and genetic testing information of a case of SP...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biopsy
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dyspnea

Share to Infant

Share to Lung Diseases, Interstitial

Share to Pulmonary Surfactant-Associated Protein C

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 23527967

Genes

SFTPC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Pulmonary surfactant protein gene mutation associated with pediatric interstitial lung disease: a case study and the review of related literature].PMID 23527967Read ↗

[I73T mutation in the pulmonary surfactant protein C gene associated with pediatric interstitial lung disease: a case study and the review of related literature].Semantic proximity Read ↗

[Familial interstitial lung disease associated with surfactant protein C gene mutation in adults: report of two cases and literature review].Semantic proximity Read ↗

Pediatric Case Report on an Interstitial Lung Disease with a Novel Mutation of SFTPC Successfully Treated with Lung Transplantation.Semantic proximity Read ↗

A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy.Semantic proximity Read ↗

Surfactant protein disorders in childhood interstitial lung disease.Semantic proximity Read ↗

[Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].Semantic proximity Read ↗

Severe Neonatal Interstitial Lung Disease Caused by a Rare Surfactant Protein C Mutation.Semantic proximity Read ↗

[Interstitial lung diseases in children of genetic origin].Semantic proximity Read ↗

Pediatric case report: successful bilateral lung transplantation performed to treat an 8-year-old girl with pulmonary interstitial fibrosis due to surfactant protein (SP)-C gene mutation.Semantic proximity Read ↗

Hereditary interstitial lung diseases manifesting in early childhood in Japan.Semantic proximity Read ↗

[Genetic disorders of surfactant].Semantic proximity Read ↗

Interstitial lung disease in children -- genetic background and associated phenotypes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.