Genetics and Cleft
The exact cause of a cleft is still unknown. A genetics evaluation may assist in obtaining a complete diagnosis and recurrence rate for a particular individual and family.
Usually multifactorial, incidence ~ 1 in 700 births
May be a feature in over 300 syndromes:
Non-syndromic recurrence risk:
Prenatal Diagnosis
Routine amniocentesis for chromosome count will not detect non-syndromic clefts
High resolution ultrasound may detect a cleft, but diagnosis incomplete
Prenatal consultation is available at our center to introduce team care and provide general information