Skip to main content
Have a personal or library account? Click to login
Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems Cover

Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems

By: S Tanriverdi,  M Polat and  H Onay  
Open Access
|Jun 2022

Figures & Tables

The symptoms and diagnoses of infants that heterozygous CFTR gene mutation was detected in the control and patient groups_

Heterozygous CFTR Gene Mutation (n=10)Symptoms of the InfantDiagnosis of the Infant
E1228G (c.3683A>G) heterozygousasymptomatichyperbilirubinemia
E217G (c.650A>G) heterozygousasymptomatichyperbilirubinemia
E632TfsX9 (c.1894_1895delAG) het.asymptomatichyperbilirubinemia
1807M (c.2421A>G) heterozygousasymptomatichyperbilirubinemia
1807M (c.2421A>G) heterozygousasymptomatichyperbilirubinemia
S573F (c.1718C>T) heterozygoussymptomatichypernatremic dyhydration
A46D (c.137C>A) heterozygoustachypnea; oxygen requirementrespiratory distress syndrome (RDS)
D1312G (c.3935A>G) heterozygoustachypnea; retractionrespiratory distress syndrome (RDS)
R117H (c.350G>A) heterozygoustachypnea; retractiontransient tachypnea of newborn
S1426P (c.4276T>C) heterozygouscough; wheezingpneumonia

Demographic characteristics of the control group and the patient group_

ParametersControl Group (n = 20)Patient Group (n = 20)p Value

Gender:
  females11111.000
  males99

Mean birth weight (g) ± SD (min-max)3278.00 ± 585.62 (1970.00–4180.00)2273.00 ± 94.63 (610.00–3850.00)0.297

Mean birth height (cm) ± SD (min-max)49.95 ± 1.80 (45.00–53.00)44.20 ± 6.37 (33.00–51.000.186

Mean head circumference (cm) ± SD (min-max)34.55 ± 1.15 (31.50–37.00)31.50 ± 3.84 (23.00–37.00)0.134

Delivery type:
  NspD500.017
  C-section1520

Gestational age (weeks)38.20 ± 1.16 (37.00–41.00)35.25 ± 4.65 (26.00–40.00)0.062

Intrauterine growth retardation (n)240.091

Median Apgar score (1st min.) (min-max)8 (7–9)7 (5–8)0.009

Median Apgar score (5th min.) (min-max)9 (9–10)8 (7–9)0.001

CFTR gene analysis of infants in the control group_

CFTR Gene AnalysisControl Group (n=20)
Normal (n)14
E1228G (C.3683A>G) het. (n)1
E217G (c.3683A>G) het. (n)1
E632TfsX9) (c.1894_1895delAG) het. (n)1
1807M (c.2421A>G) het. (n)2
S573F (c.1718C>T) het. (n)1

Pathologies and treatments of infants in the patient group_

ParametersPatient Group (n = 20)

Respiratory distress syndrome (RDS) (n)9

Congenital pneumonia (n)2

Pneumonia (n)4

Transient tacypnea of newborn (n)5

Surfactant treatment (n)5

Mechanical ventilation treatment (n)11

Mean duration of mechanical ventilation (days)2.25 ± 4.49 (1.00–20.00)

nCPAP treatment (n)13

Mean duration of nCPAP (days)9.10 ± 15.43 (1.00–51.00)

Oxygen treatment (n)17

Mean duration of oxygen therapy (days)13.35 ± 20.71 (1.00–66.00)

Bronchopulmonary dysplasia (BPD) (n)3

Steroid treatment (n):
  IV0
  inhaled5

Patent ductus arteriosus (n)4

Pulmonary hypertension (n)1

Sepsis (n):
  clinical18
  proven2

Intraventricular hemorrhage (n)1

Mean length of stay in hospital (days)24.65 ± 21.32 (9.00–71.00)

CFTR gene analysis of infants in the patient group_

CFTR Gene AnalysisPatient Group (n=20)
Normal (n)16
A46D (c.137C>A) het. (n)1
D1312G (c.3935A>G) het. (n)1
R117H (c.350G>A) het. (n)1
S1426P (c.4276T>C) het. (n)1

Symptoms and signs of respiratory distress in the patient group_

SymptomsPatient Group (n=20)
Cough4
Wheezing5
Grunting10
Apnea3
Tachpnea19
Retraction15
Rales/rhonchi12
Prolonged expiration1
Tachycardia2
Oxygen requirement17
Hypotonia6
Language: English
Page range: 25 - 31
Published on: Jun 5, 2022
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2022 S Tanriverdi, M Polat, H Onay, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.