
CASE REPORT OF A SUCCESSFUL PREGNANCY
IN A CYSTIC FIBROSIS PATIENT WITH THE
c.1521_1523delCTT/c.3718-2477C>T GENOTYPES Spasova VL, Koleva LI, Toncheva DI, Karamisheva VI *Corresponding Author: Victoria L. Spasova, M.D., Department of Medical Genetics, Medical University
of Sofia, 2 Zdrave Str., 1431 Sofia, Bulgaria. Tel: +359-887-06-65-87. Fax: +359-9520-357.
E-mail: vic.spasova@ gmail.com page: 103
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INTRODUCTION
Cystic fibrosis (CF) is a genetic disorder inherited in
an autosomal-recessive manner. It is caused by a mutation
in the CFTR gene, which codes for a chloride transporter
found on the surface of the epithelial cells that line the
exocrine glands. Reduced chloride conductance results
in thick secretions that damage the respiratory system,
pancreas, reproductive system and hepatobiliary ducts.
Cystic fibrosis is the most common inherited disease in
Caucasian populations, with an incidence of 1/2500 newborns
[1]. Cystic fibrosis carrier frequency in Bulgaria
is 1/33, meaning that 1/3600 newborns are affected [2].
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