Weismann Netter Stuhl Syndrome
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Weismann Netter Stuhl 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.
- Anterior Bowing of the Legs with Dwarfism
- Skeletal Dysplasia, Weismann Netter Stuhl Type
- Toxopachyosteose Diaphysaire Tibio-Peroniere
- Weismann-Netter Syndrome
Weismann-Netter-Stuhl syndrome is an extremely rare inherited skeletal disorder characterized by the abnormal development of bone (osseous dysplasia). Affected individuals exhibit bowing of the long portions (shafts) of the shinbone (tibia) and the outer, smaller bone of the leg below the knee (fibula). In some individuals, other bones may also be affected, such as the ribs, pelvis, spinal column, and/or bones in the arms. The primary characteristic of Weismann-Netter-Stuhl syndrome is short stature (dwarfism). In most cases, this disorder is thought to be inherited as an autosomal dominant trait.
Human Growth Foundation
997 Glen Cove Avenue
Glen Head, NY 11545
Little People of America, Inc.
250 El Camino Real Suite 201
Tustin, CA 92780
Coalition for Heritable Disorders of Connective Tissue (CHDCT)
4301 Connecticut Avenue, NW Suite 404
Washington, DC 20008
NIH/National Institute of Child Health and Human Development
31 Center Dr
Building 31, Room 2A32
Bethesda, MD 20892
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
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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
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Last Updated: 4/18/2008
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