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Genetic and Rare Diseases Information Center (GARD)

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Beta ketothiolase deficiency

Other Names for this Disease
  • 2-methyl-3-hydroxybutyricacidemia
  • 3-ketothiolase deficiency
  • 3-oxothiolase deficiency
  • Alpha-methylacetoaceticaciduria
  • Mitochondrial acetoacetyl-CoA Thiolase deficiency
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Your Question

A young family has a 3 year old girl with this disease. The parents would like to have additional children but are afraid to have another affected baby. What are their options?

Our Answer

We have identified the following information that we hope you find helpful. If you still have questions, please contact us.

What options are available for a couple that has child with beta ketothiolase deficiency who want to have a healthy baby?

Couples who are at high risk for having a child with beta ketothiolase deficiency have several options that may be available either before a pregnancy or during a pregnancy. The optimal time to determine genetic risk, clarify carrier status of parents, and discuss the availability of prenatal testing is before pregnancy. Genetic counseling (which includes a discussion of potential risks to offspring as well as reproductive options) is recommended for individuals who are affected, are carriers, or are at risk of being carriers for genetic disorders.

Finding out the genetic status of the fetus during a pregnancy for pregnancies at high risk (i.e. those at 25% risk based on family history) is possible either by analyzing T2 activity (the defective enzyme in the disorder) or by detecting mutations in fetal DNA.[1] These tests can be performed following either chorionic villus sampling (CVS) between approximately 10 and 12 weeks gestation, or amniocentesis usually between 15 and 18 weeks gestation. For couples seeking DNA analysis to identify whether the fetus has inherited specific disease-causing mutations, the mutations in an affected family member or in the carrier parents must be known before prenatal testing can be performed.

As an alternative to prenatal diagnosis during the pregnancy, preimplantation genetic diagnosis (PGD) may be available months before a pregnancy begins if the disease-causing mutations have been identified. Preimplantation diagnosis is done following in vitro fertilization (IVF) to diagnose a genetic disease in an embryo before it is introduced into the uterus. When doing PGD, laboratories can test a single cell from an embryo that is just days old. Besides testing for the specific disorder in question, PGD can also provide information about whether the embryo is male or female and whether it is carrying chromosomal abnormalities or rearrangements.[2]

GeneTests lists the names of laboratories that are performing testing for beta ketothiolase deficiency. Please note that most of the laboratories listed through GeneTests do not accept direct contact from patients and their families; therefore, if you are interested in learning more, you will need to work with a health care provider or a genetics professional. To view the contact information for the clinical laboratories conducting testing (including prenatal diagnosis), click here. For a list of laboratories that offer PGD, click here.
Last updated: 10/23/2011

How can I find a genetics professional in my area?

Genetics clinics are a source of information for individuals and families regarding genetic conditions, treatment, inheritance, and genetic risks to other family members. More information about genetic consultations is available from Genetics Home Reference. To find a genetics clinic, we recommend that you contact your primary healthcare provider for a referral.

The following online resources can help you find a genetics professional in your community:
Last updated: 10/18/2013