The most surprising finding was that none of the parents who took part had a clear understanding of recurrence risks, despite being born with a cleft themselves.
Lawrence, Kansas (PRWEB) July 14, 2015
Every three minutes a baby is born with a cleft lip and/or palate, making it one of the most common congenital conditions in the world. In Western society, the main surgery is performed within the first year of life, while dental care, speech therapy, physiological care, further oral surgeries and so on is ongoing up to approximately 18 years old. However, a recent study conducted found that people with a cleft lip/palate condition were unaware of it as a hereditary condition and the increased risk of passing it along to their children.
A study was carried out as part of the world's largest cleft lip and palate research program, The Cleft Collective, which aims to identify the causes of cleft, the best treatments for cleft and appropriate psychological support for those affected (http://www.cleftcollective.org.uk). The study was described in the article “Starting a Family: The Experience of Parents With Cleft Lip and/or Palate,” in The Cleft Palate-Craniofacial Journal discussing 24 parents with cleft lip/palate whose children were born with or without the condition. The parents were given the opportunity to discuss their feelings and reactions to the birth of their child and learning of their condition for the first time.
The research conducted was comprised mainly of one-on-one, in-depth interviews with the participants. There was some mixed feedback from people who either felt a rejuvenation to return to treatment after seeing their children and those who felt a new sense of trauma in reliving all their painful memories. Also, while some parents felt guilt for passing along their condition, there was a genuine feeling that because they themselves experienced the same condition, they were well-equipped to help guide their children through childhood and the difficulties they would face. This gives an overall feeling that with the right support in place, this does not have to be a debilitating congenital condition.
In doing this research, author Nicola Stock felt, “The most surprising finding was that none of the parents who took part had a clear understanding of recurrence risks, despite being born with a cleft themselves. Accurate information and access to genetic counselling is therefore vital for young people born with heritable conditions such as cleft lip/palate, who are prospective parents. In addition, research into the genetic and environmental causes of conditions such as cleft are crucial for education and prevention.” The authors do believe that more support is needed for young adults with a cleft palate condition after they reach the age of 18, especially when they are deciding to start families; they should be fully informed of the hereditary impact of their condition.
Full text of the article, “Starting a Family: The Experience of Parents With Cleft Lip and/or Palate,” The Cleft Palate–Craniofacial Journal, Vol. 52, No. 4, 2015, is now available online.
About The Cleft Palate–Craniofacial Journal
The Cleft Palate–Craniofacial Journal is an international, interdisciplinary journal reporting on clinical and research activities in cleft lip/palate and other craniofacial anomalies, together with research in related laboratory sciences. It is the official publication of the American Cleft Palate–Craniofacial Association (ACPA). For more information, visit http://www.acpa-cpf.org/.