A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
Author(s) -
Tovi M. Anderson,
Allison Buterbaugh,
Kaitlin M. Love,
Jeannie Visootsak
Publication year - 2013
Publication title -
case reports in genetics
Language(s) - English
Resource type - Journals
eISSN - 2090-6544
pISSN - 2090-6552
DOI - 10.1155/2013/504695
Subject(s) - fragile x syndrome , medicine , fragile x , intellectual disability , pediatrics , down syndrome , psychiatry , genetics , gene , biology
Down syndrome is the most common identifiable genetic cause of intellectual disability, with a unique physical gestalt that makes diagnosis possible during the newborn period. However, the physical characteristics of Fragile X syndrome are fairly subtle, resulting in the first clinical suspicion often arising from delayed developmental milestones. In addition, maladaptive behavior and autistic-like tendencies, such as hand flapping, poor eye contact, and hand biting, may be noted in Fragile X syndrome but are not as commonly observed in Down syndrome. Recognition of a potential secondary diagnosis, such as Fragile X syndrome, in individuals with Down syndrome is critical because there have been advances in targeted pharmacologic treatments for both conditions. Thus, an accurate diagnosis has implications in improving the individual's quality of life.
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