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Infantile Cortical Hyperostosis / Caffey-Silverman disease

Last Updated on Apr 19, 2013
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Introduction

Infantile Cortical Hyperostosis is an unusual disease of an unknown etiology. It is also known as Caffey's disease or Caffey-Silverman disease after the persons who discovered it. The main feature of the disease is a peculiar cortical thickening of certain bones like the mandible, the clavicles, and the shafts of long bones.

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Several other diseases like syphilis, scurvy, rickets and traumatic injury also produce cortical thickening in bones, but as yet researchers have been unable to find any link between these diseases and infantile cortical hyperostosis.

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Latest Publications and Research on Infantile Cortical Hyperostosis


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Post a Comment

Comments should be on the topic and should not be abusive. The editorial team reserves the right to review and moderate the comments posted on the site.

Comments

aslampasha

my baby sarah fought brilliantly against all odds but she could not tolerate the hospitalized infection(septicemia)and died on 8th nov 09.she was admitted for caffeys symptoms but got infected,drs says this that,but i would say one thing before admission drs should know the patient or else why they have admitted my kid,simply to study the case or they dont want to loose study material.end of the day i have lost my darling.
Sayed Aslam
Hubli
india

aslampasha

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.

aslampasha

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

thevagi

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

Annie0909

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...

aslampasha

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.....

guest

Similar experience-your son is over a year now,how is he getting on?

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