Cornelia de Lange Syndrome (CdLS)
A young new couple decides the honeymoon is over and decides they want to bring children into this world. After trying numerous times unsuccessfully they finally got positive results that a baby is on the way. Through out the pregnancy problems would arise and tests would show that the baby was going to be born with birth defetc s. More tests would have to be done after birth to get an accurate diagnosis. After months of horrible complications and negative doctor visits a baby boy was born into this world.
Upon being brought into this world, the little boy named Brayden was diagnosed with many different conditions. Doctors knew were all of these were linked together some how but no one had a name for it. Test would go on and weekly doctors visits were attended but now one could say what was wrong with this baby they just knew he was different. Two years into Brayden's life he was diagnosis with a condition called the Cornelia de Lange Syndrome (CdLS).
Finally having a diagnosis meant tons to the parents of this boy, they could now become educated and informed, along with becoming more knowledgeable on how to take care of this bundle of joy.
As with most syndromes CdLS is not commonly associated with a definition. However the most scientific definition I have found states that CdLS is a disorder of unknown etiology resulting in a syndrome characterized by specific dysmorphic features.
In 1933, Dr. Cornelia de Lange, a Dutch pediatrician, described two children with similar features, one 17 months and the other 6 months, who were admitted within weeks of each other to Emma Children's Hospital. The first child had pneumonia. Her first year of life had been characterized by a lot of feeding difficulties and she was very small for her age, with a proportionately smaller head circumference.
Other unusual facial characteristics were noted be Dr. de Lange. Soon after this child was discharged, a second...