We are planning a child with my husband, but we are wondering because my husband has clubfoot (shorter limbs, smaller foot), his cousin has the same. Is this a genetic defect, can our child also have such a foot? Is there any research to rule out it's genetics?
If a limb defect occurred in 2 people in the family, it is most likely genetically determined. However, the subject and scope of genetic testing must be discussed at the Genetic Clinic, taking into account symptoms and family history.
Remember that our expert's answer is informative and will not replace a visit to the doctor.
Prof. extra Aleksandra Jezela-Stanek, MD, PhDHe has been specializing in clinical genetics for several years. Currently, he is an associate professor at the Children's Memorial He alth Institute in Warsaw. Permanently associated with Silesia where, among others in cooperation with testDNA Laboratorium Sp. z o.o. provides telephone consultations to patients who want to discuss the results of genetic tests or talk about the transmission of genetic diseases in the family. In practice, he deals with the diagnosis of genetic causes of birth defects, developmental disorders and pregnancy failures.
Patients have the opportunity to obtain information on the effects of a given DNA test result, the need to take preventive measures and indicate tests necessary to perform and then diagnose the disease. Ms Docent is appreciated not only for her knowledge and professionalism, but also for a nice disposition towards patients, which was often emphasized by them on internet forums.
More advice from this expert
Genetically Testing After Miscarriages [Expert Advice]Close parentage and the necessity of amniocentesis [Expert advice]I want to grow even more. Which doctor should I see? [Expert advice]Pregnancy after 40 and after thrombosis. What genetic tests? [Expert advice]Is drug-induced hearing loss hereditary? [Expert advice]Is varus hereditary? [Expert advice]Do you have to wait for a karyotype test? [Expert advice]Inheritance of pigmentary retinitis [Expert Advice]Inheriting thrombophilia [Expert Advice]Sperm DNA fragmentation and the risk of miscarriage [Expert advice]Genetically determined spongif.webporm cardiomyopathy [Expert Advice]Blood group. Negative for parents and positive for a child? [Expert advice]How to check cancer predisposition? [Expert advice]Folic acid and vitamin B12 and the MTHFR mutation [Expert's tip]Literature on the diagnosis of genetic diseases [Advice of an expert]MTHFR gene mutation and subsequent pregnancy [Expert's advice]MTHFR gene mutation, miscarriage and subsequent pregnancy [Expert's advice]Factor V Leiden and PAI 1 mutation and pregnancy [Expert's advice]Gene mutations and the risk of thrombosis [Expert advice]Planning pregnancy and the likelihood of mental retardation [Expert's advice]Elevated HE4 and a family history of ovarian cancer [Expert Advice]Gene polymorphism and the possibility of termination of pregnancy [Expert's advice]Single-sex miscarriages [Expert Advice]Spontaneous miscarriage. How to determine its cause? [Expert advice]Positive karyotype and the possibility of a genetic disease [Expert's advice]The likelihood of genetic defects and the next pregnancy [Expert's advice]Varus in 2 people in the family. Is it a genetic defect? [Expert advice]Papp's test. What does trisomy 21 risk adjusted risk 1: 682 mean? [Expert advice]Negative parental blood group and positive child? [Expert advice]Cousin's grandchildren and the risk of genetic defects [Expert's advice]