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

被引：5

作者：

Wilkes, Courtney ^{[1
]}

Graetz, Melissa ^{[2
]}

Downie, Lilian ^{[2
]}

Bethune, Michael ^{[3
,4
]}

Chong, David ^{[1
]}

机构：

[1] Royal Childrens Hosp, Dept Plast & Maxillofacial Surg, Melbourne, Vic, Australia

[2] Mercy Hosp Women, Dept Genet, Melbourne, Vic, Australia

[3] Mercy Hosp Women, Dept Med Imaging & Perinatal Med, Melbourne, Vic, Australia

[4] Specialist Womens Ultrasound, Melbourne, Vic, Australia

来源：

PRENATAL DIAGNOSIS | 2023年 / 43卷 / 10期

关键词：

OROFACIAL CLEFTS; ORAL CLEFTS; BIRTH-DEFECTS; ASSOCIATION; PREVALENCE; MANAGEMENT;

D O I：

10.1002/pd.6418

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Cleft 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.

引用

页码：1310 / 1319

页数：10

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