APoGI for the Haemoglobin Disorders

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Implications for a Child when One Partner carries Haemoglobin S (Sickle Cell) and the Other carries Haemoglobin O Arab

This couple could have a child with haemoglobin S/O Arab disorder.

Partner who carries haemoglobin S Partner who carries haemoglobin O Arab
Not a carrier Carrier of haemoglobin S Carrier of haemoglobin O Arab Child with haemoglobin S/O Arab disorder

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 S/O Arab disorder.

Haemoglobin S/O Arab disorder...

...is a sickle cell disorder. It is rare, and we are not able to describe it with complete confidence. It is generally thought to be a mild type of sickle cell disorder. Children with a sickle cell disorder have an increased risk of serious infections, and need to take antibiotics daily. Some people with haemoglobin S/O Arab disorder are completely healthy all their life. Some are anaemic, and have attacks of severe pain in joints or other parts of the body from time to time. A few have severe health problems and need frequent admissions to hospital. People with haemoglobin S/O Arab disorder should attend a sickle cell clinic regularly for a check-up and advice.

At present, it is not possible to predict whether a particular couple could have children with mild, moderate or severe haemoglobin S/O Arab disorder.

It is possible to test a baby for Haemoglobin S/O Arab disorder 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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