Prenatal diagnosis of cleft lip and/or palate: What do we tell prospective parents?

Author:

Wilkes Courtney1ORCID,Graetz Melissa2,Downie Lilian2,Bethune Michael34,Chong David1

Affiliation:

1. Department of Plastic and Maxillofacial Surgery The Royal Children's Hospital Melbourne Victoria Australia

2. Department of Genetics Mercy Hospital for Women Melbourne Victoria Australia

3. Department of Medical Imaging and Perinatal Medicine The Mercy Hospital for Women Melbourne Victoria Australia

4. Specialist Women's Ultrasound Melbourne Victoria Australia

Abstract

AbstractCleft lip and/or palate (CL/CP) is the most common congenital craniofacial anomaly and parents often ask, “how did this happen?” Patients and families may benefit from access to a multidisciplinary team (MDT) from prenatal diagnosis into early adulthood. Multiple factors can contribute to the development of a cleft. We discuss the epidemiology and risk factors that increase the likelihood of having a newborn with a cleft. The purpose of this article is to review the prenatal investigations involved in the diagnosis and workup of these patients in addition to postpartum treatment, prognostic factors, and counseling families regarding future recurrence risk.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

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