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21 Nov 2005

neurofibroma
My husband had a neurofibroma (only one when he was in high school and which was removed) in the location of his neck vertebrae which eventually led to damage of some of the nerves of his left side so that he has very little use of his left hand and also has a little trouble walking. He hasnt had a repeat of this eversince (i.e. for 20 years) What is the chances of our baby developing this? As far as I know there is no other abnormalities in the rest of his family except his maternal grandmother had a white patch in her hair. Has this got anything to do with a neurofibroma?
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Expert
Geneticist
geneticist

01 Jan 0001

Dear Ellie

I was sorry to learn about your husband's NF problems. The condition is very variable, but it is unlikely that the grandmother's white hair patch is a manifestation of NF. Assuming that your husband has NF rather than just an isolated neurofibroma, the chances of any child fathered by him inheritng the NF gene would be 50/50. Your paediatrician could check out your baby for any early signs of NF.

Regards, Maritha & Genecare Consultant Medical Geneticist
The information provided does not constitute a diagnosis of your condition. You should consult a medical practitioner or other appropriate health care professional for a physical examination, diagnosis and formal advice. Health24 and the expert accept no responsibility or liability for any damage or personal harm you may suffer resulting from making use of this content.
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