ATP-binding cassette transporter A3 (ABCA3) mutation in a late preterm with respiratory distress syndrome.
نویسندگان
چکیده
BACKGROUND Surfactant protein abnormalities are rare causes of respiratory distress syndrome. CASE CHARACTERISTICS A late preterm (36 wks) who presented with respiratory distress syndrome. OBSERVATION He was found to be a homozygous for a G to T transversion at the first base in intron 24, of ABCA3 gene which is necessary for lamellar body formation and surfactant production. OUTCOME He died of severe respiratory failure even after multiple doses of surfactants and ventilation. MESSAGE Surfactant deficiency with ABCA3 gene mutation needs to be suspected in late preterms who present with respiratory distress syndrome.
منابع مشابه
Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.
OBJECTIVE To determine whether synonymous variants in the adenosine triphosphate-binding cassette A3 transporter (ABCA3) gene increase the risk for neonatal respiratory distress syndrome (RDS) in term and late preterm infants of European and African descent. STUDY DESIGN Using next-generation pooled sequencing of race-stratified DNA samples from infants of European and African descent at ≥34 ...
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عنوان ژورنال:
- Indian pediatrics
دوره 51 7 شماره
صفحات -
تاریخ انتشار 2014