Familial diseases revealed by a fetal anomaly.

The recognition of a fetal anomaly can lead to the same diagnosis being made in one of the asymptomatic parents unaware of the problem. We analyzed cases in which the discovery of a fetal anomaly led to the discovery of a genetic familial disorder.
Families in which the recognition of a fetal anomaly led to the same diagnosis being made in one of the asymptomatic parents were included.
Twenty couples were included in the study. The fetal anomalies were cleft lip and palate (4), cardiac anomalies (2), cerebral anomalies (1), bilateral club feet with polyhydramnios, akinesia or camptodactily (5), nuchal anomalies (2), micromelia (3), polydactyly (2), and limited elbow extension (1). Genetic counselling helped establish nine maternal diseases as follows: Steinert disease (3), spinal muscular atrophy (1), antecubital pterygium (1), DiGeorge (1), Wardenburg type II (1), Charge (1) and Greig syndromes (1). Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1). Twelve couples continued with pregnancy and eight opted for termination of pregnancy.
The fetus is central in giving the first insight into a familial disorder. It can reveal familial diseases undiscovered in the parent and help understand the mode of transmission of an anomaly, mainly the autosomal dominant diseases with variable expressions.
AuthorsR Robyr, J-P Bernard, J Roume, Y Ville
JournalPrenatal diagnosis (Prenat Diagn) Vol. 26 Issue 13 Pg. 1224-34 (Dec 2006) ISSN: 0197-3851 [Print] England
PMID17139695 (Publication Type: Journal Article)
CopyrightCopyright (c) 2006 John Wiley & Sons, Ltd.
  • Abnormalities, Multiple (diagnosis, genetics)
  • Family Health
  • Female
  • Fetus (abnormalities)
  • Genetic Counseling
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Gestational Age
  • Humans
  • Male
  • Prenatal Diagnosis

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!

Choose Username:
Verify Password: