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Survival of an infant with homozygous surfactant protein C (SFTPC) mutation.

Identifieur interne : 000231 ( Ncbi/Curation ); précédent : 000230; suivant : 000232

Survival of an infant with homozygous surfactant protein C (SFTPC) mutation.

Auteurs : Zeynep Ar Kan-Ayy Ld Z [Turquie] ; Sule Caglayan-Sozmen ; Sakine Is K ; Robin Deterding ; Megan K. Dishop ; Remy Couderc ; Ralph Epaud ; Malek Louha ; Nevin Uzuner

Source :

RBID : pubmed:24347240

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English descriptors

Abstract

Lung diseases caused by surfactant protein C (SFTPC) mutations are inherited as autosomal traits with variable penetrance and severity or as sporadic disease caused by a de novo mutation on one allele. Here, we report the case of a child surviving with a homozygous surfactant protein C mutation after aggressive clinical management unlike his six siblings who died in infancy. This presentation raises the suspicion of an autosomal recessive inheritance that is discussed in this report.

DOI: 10.1002/ppul.22976
PubMed: 24347240

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pubmed:24347240

Le document en format XML

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<nlm:affiliation>Faculty of Medicine, Department of Pediatric Allergy and Pulmonology, Dokuz Eylul University, Izmir, Turkey.</nlm:affiliation>
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<term>Azithromycin (therapeutic use)</term>
<term>Consanguinity</term>
<term>Genes, Recessive</term>
<term>Homozygote</term>
<term>Humans</term>
<term>Hydroxychloroquine (therapeutic use)</term>
<term>Infant</term>
<term>Lung (diagnostic imaging)</term>
<term>Lung (pathology)</term>
<term>Lung (ultrastructure)</term>
<term>Male</term>
<term>Methylprednisolone (therapeutic use)</term>
<term>Microscopy, Electron</term>
<term>Mutation, Missense (genetics)</term>
<term>Oxygen Inhalation Therapy</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Pulmonary Alveolar Proteinosis (diagnosis)</term>
<term>Pulmonary Alveolar Proteinosis (genetics)</term>
<term>Pulmonary Surfactant-Associated Protein C (genetics)</term>
<term>Radiography</term>
<term>Respiration, Artificial</term>
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<term>Fratrie</term>
<term>Gènes récessifs</term>
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<term>Humains</term>
<term>Hydroxychloroquine (usage thérapeutique)</term>
<term>Microscopie électronique</term>
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<term>Poumon (anatomopathologie)</term>
<term>Poumon (imagerie diagnostique)</term>
<term>Poumon (ultrastructure)</term>
<term>Protéine C associée au surfactant pulmonaire (génétique)</term>
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<term>Protéinose alvéolaire pulmonaire (génétique)</term>
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<term>Pulmonary Alveolar Proteinosis</term>
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<term>Respiratory Distress Syndrome, Adult</term>
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<term>Lung</term>
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<term>Anti-inflammatoires</term>
<term>Antibactériens</term>
<term>Azithromycine</term>
<term>Hydroxychloroquine</term>
<term>Méthylprednisolone</term>
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<term>Consanguinity</term>
<term>Genes, Recessive</term>
<term>Homozygote</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Microscopy, Electron</term>
<term>Oxygen Inhalation Therapy</term>
<term>Pedigree</term>
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<term>Radiography</term>
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<term>Treatment Outcome</term>
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<term>Consanguinité</term>
<term>Fratrie</term>
<term>Gènes récessifs</term>
<term>Homozygote</term>
<term>Humains</term>
<term>Microscopie électronique</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Oxygénothérapie</term>
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<term>Phénotype</term>
<term>Radiographie</term>
<term>Résultat thérapeutique</term>
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<front>
<div type="abstract" xml:lang="en">Lung diseases caused by surfactant protein C (SFTPC) mutations are inherited as autosomal traits with variable penetrance and severity or as sporadic disease caused by a de novo mutation on one allele. Here, we report the case of a child surviving with a homozygous surfactant protein C mutation after aggressive clinical management unlike his six siblings who died in infancy. This presentation raises the suspicion of an autosomal recessive inheritance that is discussed in this report.</div>
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