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Rom J Morphol Embryol ; 60(2): 667-671, 2019.
Article in English | MEDLINE | ID: mdl-31658342

ABSTRACT

Cystic fibrosis (CF) is a multi-system autosomal recessive disorder, results of mutations in the CF transmembrane conductance regulator (CFTR) gene, located on the long arm of chromosome 7. We present a special family couple with particular medical history of CF, who comes to our Clinic for genetic tests and a prenatal genetic counseling, to prevent the birth of a new affected CF child. Genetic analysis showed that the first affected child, a daughter, is compound heterozygous for two clinically significant recessive mutations: c.1521_1523delCTT; p.Phe508del, inherited from her mother, who carries the same CFTR mutation, and c.1853_1863delTTTTGCATGAA; p.IIe618Argfs 2, inherited from her father, who is heterozygous, healthy carrier, for the same CFTR mutation. In our case report, early prenatal genetic testing, pre- and post-test genetic counseling was crucial in the management of the present pregnancy, to prevent the birth of a new affected CF child.


Subject(s)
Cystic Fibrosis/diagnosis , Cystic Fibrosis/prevention & control , Fetus/pathology , Genetic Testing/methods , Prenatal Diagnosis/methods , Adult , Cystic Fibrosis/genetics , Female , Humans , Male , Mutation , Pregnancy
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