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[Ed. Note:
The opinions expressed below are solely those of the author. They do
not represent the opinions of the editor, publisher, or this publication.
Anyone with a medical problem is strongly encouraged to seek professional
medical care.]
I am a board
certified pediatrician practicing in West Palm Beach, FL. I was diagnosed
with Chari malformation in July, 1988 and have undergone a
cervico-syringoarachnoid shunt in 1990 and decompression surgery in 2003. I
take medications daily to enable me to be present for my patients. I hope
that in this monthly article series that I might “bridge the gap” between
patient and doctor.
November 20, 2006 --
Connective tissue is the foundation of our bodies. It is found in the
muscles, the bones, the walls of blood vessels, and the skin. Some of us
with Chiari 1 malformation (CM1) have been told that we have cerebellar
tonsillar herniation into our spinal column because our posterior cranial
fossa is too small—an abnormality of bones in our skull. Some Chiari
patients have other bony abnormalities of the skull or spine—deformities of
the odontoid process (anterior part of the second cervical vertebra), bifid
or posterior split in the first cervical vertebra), fusion of first cervical
vertebra to the skull, fusion or abnormal bony joining of cervical vertebrae
(known as Klippel Feil anomaly), cranial lacunae or unexpected holes in the
cranial bones. Some Chiarians have abnormal facial structures—small sinuses
with frequent infections, temperomandibular joint problems (TMJ) or small
mandibles (difficulty in jaw opening).
In 2005 at the American Syringomyelia Alliance Project (ASAP) and the Ehler
Danlos Syndrome (EDS) conferences, Dr. Thomas Milhorat, Director of The
Chiari Institute at North Shore LIJ in Great Neck New York and Dr. McDonnell
of the genetics laboratory of the National Institute of Aging at the
National Institute of Health in Maryland, discussed an apparent linkage
between EDS (a group of connective tissue disorders) and Chiari 1
malformation. According to their data the incidence of Chiari 1 malformation
is 1:5000 and the incidence of Ehler Danlos Syndromes is 1:5000. If these
two entities were random, you would expect them to occur together (multiply
the two numbers) in 1 in 25 million. However Dr. Milhorat reports that he
sees at the Chiari Institute in New York, an incidence of 1 in 15
patients of simultaneous CM1 and EDS.
EDS patients usually demonstrate one or more of the following
components—hyper-elastic and fragile skin with frequent atrophic scarring,
hyper mobility of joints (double-jointed or frequent dislocations), and/or
fragility of cutaneous blood vessels (easy bruising) or abnormalities of
major blood vessels (aneurysms). Collagens are the main proteins of
connective tissue and defects in various collagens have been discovered for
several types of EDS. Defects can happen in the quantity (amount of collagen
molecules produced) or in the quality of the collagen (abnormal collagen
types produced).
Dr. Milhorat at that conference discussed that the patients that presented
with both EDS and CM1 appeared to have more symptoms relating to anterior
brainstem dysfunction including nausea, dysphagia, hoarseness, sleep apnea,
difficulty swallowing, dysautonomia (sometimes known as POTS), palpitations
and shortness of breath. Their radiographic findings were more likely to
show pannus formation around the odontoid and the aforementioned cranial
abnormalities and facial abnormalities. Patients with both syndromes were
more likely to demonstrate swallowing problems post-operatively and were
more likely to demonstrate cranio-cervical instability.
Dr. McDonnell went on to discuss the known genetic defects in some types of
EDS while the specific gene defects had not been identified in other types.
Familial aggregation studies (families with multiple cases of illness)
suggest genetic causes for EDS and CM1 even though the specific genes
affected nor their mechanisms of action have not been determined.
For further information on this subject, the Chiari Institute has posted a
link on its website where the talks can be watched in their entirety. Go to
their site
http://www.northshorelij.com/body.cfm?ID=6407
then click on VIDEOS
then click on Ehlers-Danlos Conference
--
Regina S. Bland, MD
** If you
would like to share your thoughts with Dr. Bland, or have ideas for her
column,
please send them to
drbland@bellsouth.net. Due to the volume and nature of email
received, individual responses are not possible. **
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