DIAG (Corrections)

[Robert Resta <bc928@scn.org>]

The most recent DIAG postings contained minor errors in Message 1 and
Message 3. The corrected postings are listed below. We apologize for any
inconveniences.


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           HUM-MOLGEN  DIAGnostics/Clinical Research
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This DIAG message contains 2 professional requests:

1) del(3)(p23)
3) Geroderma osteodyplastica and agenesis of the corpus callosum



Carlo Gambacorti, MD, Editor
Harker Rhodes, MD, Assistant Editor
Robert Resta, MS, Editor

                       Human Molecular Genetics Network
                       Diagnostics/Clinical Research Section
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1) del(3)(p23)

We have a patient with a deletion of the tip of the short arm of the third
chromosome i.e. del(3)(p23). The family is interested in meeting/talking
with other families with similar conditions.


N.J. Leonard
Assistant Professor
Medical Geneticist
Clinical Sciences Building B-139
University of Alberta
Edmonton, Alberta
CANADA T6G 2B7
phone (403) 492-4077
fax (403) 492-6845
****PLEASE NOTE NEW EMAIL ADDRESS ****
email norma.leonard@ualberta.ca

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3) Geroderma osteodyplastica and agenesis of the corpus callosum

I am a Physical Therapist Assistant student and have been working with a young
boy with the autosomal recessive disorder geroderma  osteodyplastica.  He also
has been diagnosed with agenesis of the corpus callosum.  I am having a
difficult time finding ANY information on these conditions.  Any help you can
give me will be greatly appreciated.

                                      Thank you.
                                       K Burdette
burdet@zoomnet.com