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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
Published by: Macedonian Academy of Sciences and Arts
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.