APoGI for the Haemoglobin Disorders
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This is an unusual combination that has not been reported in the literature. The following information is based on general experience with these types of thalassaemia, and available scientific knowledge.
This couple could have a child with haemoglobin O Arab/Lepore thalassaemia.
Partner who carries haemoglobin Lepore thalassaemia | Partner who carries haemoglobin O Arab | ||
Not a carrier | Carrier of haemoglobin Lepore thalassaemia | Carrier of haemoglobin O Arab | Child with haemoglobin O Arab/Lepore Thalassaemia |
In each pregnancy, there are four possibilities:
In each pregnancy there is a 3 out of 4 chance of a healthy child, and a 1 out of 4 chance of child with haemoglobin O Arab/Lepore thalassaemia.
... is a form of haemoglobin O Arab/beta thalassaemia. This is a type of inherited anaemia. Many people with haemoglobin O Arab/beta thalassaemia are healthy all their life, but some are anaemic and need extra care. Current scientific knowledge suggests that a child with haemoglobin O Arab/ Lepore thalassaemia will have a mild form of haemoglobin O Arab/beta thalassaemia. However, we cannot reliably predict whether any given couple could have children with mild or more severe haemoglobin O Arab/Lepore thalassaemia.
It is possible to test a baby for Haemogobin O Arab/Lepore thalassaemia early in pregnancy. This couple should see an expert counsellor in haemoglobin disorders to discuss their options. They should do this before starting a pregnancy, or as early in pregnancy as possible.
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These documents are part of the APoGI May 1998 (Evaluation) Release and are made available subject to the APoGI Disclaimers covering usage, distribution and copying.
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