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

Neonatal respiratory failure associated with mutation in the surfactant protein C gene.

Journal of perinatology : official journal of the California Perinatal Association - 1 Jan 2006

Soraisham A S, Tierney A J, Amin H J

Abstract excerpt

We report on a term newborn with an unusual presentation and course of a rare lung disease due to mutation in SFTPC gene. This particular SFTPC mutation is novel, and the infant's lung disease was unusually severe compared to what has been previously reported in association with SFTPC mutations.

Read the complete abstract on PubMed

Topics

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

Share to Fatal Outcome
Share to Infant, Newborn
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pulmonary Surfactant-Associated Protein C

Share to Pulmonary Surfactants

Share to Radiography

Share to Respiration, Artificial

Share to Respiratory Distress Syndrome, Newborn

Source

Identifiers

PMID: 16355106
DOI: 10.1038/sj.jp.7211417

Genes

SFTPC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16355106-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neonatal respiratory failure associated with mutation in the surfactant protein C gene.PMID 16355106Read ↗

Neonatal respiratory failure due to a novel mutation in the surfactant protein C gene.Semantic proximity Read ↗

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

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

Persistent Respiratory Distress in the Term Neonate: Genetic Surfactant Deficiency DiseasesSemantic proximity Read ↗

Survival of an infant with homozygous surfactant protein C (SFTPC) mutation.Semantic proximity Read ↗

Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene.Semantic proximity Read ↗

SFTPC gene mutation p.R167Q in a premature infant.Semantic proximity Read ↗

Non-invasive management of infants with SFTPC pathogenic variantsSemantic proximity Read ↗

Towards personalized therapies for genetic disorders of surfactant dysfunction.Semantic proximity Read ↗

Child Interstitial Lung Disease in an Infant with Surfactant Protein C Dysfunction due to c.202G>T Variant (p.V68F).Semantic proximity Read ↗

[Genetic disorders of surfactant].Semantic proximity Read ↗

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