Infantile Cortical Hyperostosis / Caffey-Silverman disease | |
Treatment of Infantile Cortical Hyperostosis |
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The condition is self-limiting and regresses on its own within a period of few weeks to months and often goes unnoticed if present in a particularly benign form. Periods of remissions and exacerbations can occur. Steroids may be of some benefit in the symptomatic management of the disease. Sometimes deformities in the affected bone persist into adulthood and if they are present on the face, then corrective surgery is required. This is again for cosmetic purposes rather than for palliative purpose. |
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Posted by:
aslampasha
Posted on: 10/28/2009 Its been 4 months ever since my daughter confirmed with Caffeys,she is on naproxen but no signs of improvement her body weight remains the same ever since her birth,her platelet count is more than 9.50 due to which drs are not giving even steroids which may further worsen her condition.she is been through severe pain and fever due to which she hardly sleeps.
Posted by:
aslampasha
Posted on: 09/24/2009 MY BABY GIRL IS CONFIRMED WITH CAFFEYS DISEASE,SHOCKING IS NO FAMILY HISTORY DRS SAYS ITS A GENETIC DISEASE AND BABY IS 3 MONTH OLD IS THERE ANY TREATMENT.......... SAYED ASLAM HUBLI. INDIA
Posted by:
thevagi
Posted on: 01/25/2009 MY BABY BOY IS HAVING CAFFEY DISEASE, NO FAMILY HISTORY OF CAFFERY, HIS BLOOD TEST SHOWS HIGH HEMOGLOBIN, HIGH PLATELES AND GOANT TROMBOCIATES CELL, HE IS NOW 15 MONTHS, RIGHT RIB , MANDIBLE AND MAXILLE SWELLING, THE SWELLINGIS ALMOST NEARLY ONE YEAR. WHAT TREATMENT DID U GIVE YOUR CHILD
Posted by:
Annie0909(Guest)
Posted on: 12/29/2008 My mother had Caffey disease, I did when I was a child, and now my baby boy also has it. I am very interested to share experiences with other patients...
Posted by:
aslampasha
Posted on: 10/16/2009 please let me know the treatment and the time period you all have taken to recover,as my 4 month old baby girl is also suffering from caffeys and her symptoms are very severe.please help me..... |
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Sayed Aslam
Hubli
india