Acta Paediatrica · 1997 · 15 citations · 5 references
MedicineGeneticsPediatricsHuman GeneticsNeonatologyPediatric PulmonologyNeonatal GeneticsNeonatal Respiratory DisordersRespiratory DiseaseRespiratory Distress In NewbornsRespiratory Distress SyndromeSurfactantsBronchoalveolar Lavage AnalysisBronchoalveolar Lavage ExaminationMutationNeonatal Respiratory Distress SyndromeNeonatal Surfactant DeficiencyRespiratory Distress RecognitionSurfactant Protein Deficiency
Two infants presenting with respiratory distress in the first 24 h of life are described. Both patients underwent extensive investigation before the diagnosis of surfactant protein B-deficiency was reached. Both children died within 2 months of birth. Parental consanguinity was known to be a feature in the first case, who proved to have a previously unrecognized mutation of the surfactant protein B gene. In the second case, a history of parental consanguinity was not sought from the Caucasian family, but was later volunteered by the parents themselves. Case 2 proved to have the "common" surfactant protein B-deficient genotype. The key to diagnosis is having a high index of suspicion in any term or near-term newborn with severe respiratory distress; parental consanguinity must be excluded. Surfactant protein B-deficiency can be readily diagnosed from bronchoalveolar lavage specimens; a simple, inexpensive procedure which is well tolerated in newborns.
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Robert J. Korst, Burkhard Bewig, Ronald G. Crystal · Human Gene Therapy · 1995 · 66 citations
Heart, heart-lung, and lung transplantation in the first year of life
Vaughn A. Starnes, Philip E. Oyer, Daniel Bernstein et al. · The Annals of Thoracic Surgery · 1992 · 37 citations
Medicine, Cardiology, Pediatrics +16