Fetal arthrogryposis—what do we tell the prospective parents?

Author:

Filges Isabel1ORCID,Jünemann Stephanie2,Viehweger Elke3,Tercanli Sevgi4

Affiliation:

1. Medical Genetics, Institute of Medical Genetics and Pathology University Hospital Basel and University of Basel Basel Switzerland

2. Pediatric Neurology and Developmental Medicine University Children's Hospital Basel UKBB and University of Basel Basel Switzerland

3. Pediatric Orthopedics, Neuro‐Orthopedics and Movement Analysis Center University Children's Hospital Basel UKBB and University of Basel Basel Switzerland

4. Center for Prenatal Ultrasound Basel and University of Basel Basel Switzerland

Abstract

AbstractArthrogryposis, also termed arthrogryposis multiplex congenita, is a descriptive term for conditions with multiple congenital contractures (MCC). The etiology is extremely heterogeneous. More than 400 specific disorders have been identified so far, which may lead to or are associated with MCC and/or fetal hypo‐ and akinesia as a clinical sign. With improved sensitivity of prenatal ultrasound and expanding prenatal diagnostic options, clinicians are tasked with providing early detection in order to counsel the prospective parents regarding further prenatal diagnostic as well as management options. We summarize the most important knowledge to raise awareness for early detection in pregnancy. We review essential points for counseling when MCC is detected in order to provide answers to common questions, which, however, cannot replace interdisciplinary expert opinion in the individual case.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

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