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Ivemark Syndrome
Important
It is possible that the main title of the report Ivemark Syndrome
is not the name you expected. Please check the synonyms listing to find
the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
- Asplenia Syndrome
- Bilateral Right-Sidedness Sequence
- Splenic Agenesis Syndrome
Disorder Subdivisions
- None
General Discussion
Ivemark syndrome is a rare progressive disorder usually evident at birth. It is characterized by the absence of a spleen, malformations of the cardiovascular system and abnormal displacement of internal organs.
Resources
Ivemark Syndrome Association
71 Milton Rd
Taunton, Intl TA1 2JQ
United Kingdom
Tel: 01823 257430
Email: ingridgladki@aol.com
For a Complete Report:
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org
Last Updated: 4/4/2005
Copyright 1989, 1999, 2005 National Organization for Rare Disorders, Inc.
WebMD Medical Reference from the National Organization of Rare Disorders
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