CareLit · DOI-Nachweis · Klinische Pädiatrie
Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C
DOI 10.1055/s-0030-1261412
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Nachweis in CareLit
Autor:innenJ Pöschl, P Ruef, M Griese, P Lohse, C Aslanidis, S Rahman, M Kichi, A Al baridi, H Pappapil, L Koch
ZeitschriftKlinische Pädiatrie
Ausgabe06/2010
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Persistent ventilator dependency with 40% to 100% FiO2 in a female baby born at term now seven months old. Objective: Due to ongoing tachypnoe, CPAP and oxygen dependency since birth and CT scan appearance a congenital defect in surfactant synthesis was evaluated. Methods: Bronchoalveolar lavage: Surfactant protein (SP-) C was reduced to about 1/7 of the amount normally present in relation to the content…
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Zitierempfehlung
J Pöschl, P Ruef, M Griese, P Lohse, C Aslanidis, S Rahman, M Kichi, A Al baridi, H Pappapil, L Koch (2010) Homozygous mutation in ABCA3 Lipid-Transporter defect (EXON 9) and low level of surfactant protein C. Klinische Pädiatrie (06). https://doi.org/10.1055/s-0030-1261412
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