Weismann-Netter syndrome
Synonyms: Anterior bowing of legs with dwarfism | WNS | Weismann-Netter-Stuhl syndrome
Weismann-Netter syndrome is a rare genetic primary bent bone dysplasia characterized by anterior diaphyseal bowing of the tibia and fibula broadening of the fibula posterior cortical thickening of both bones and short stature. Additional skeletal abnormalities include scoliosis with marked lumbar lordosis horizontal sacrum and square iliac wings and/or less frequently vertebral malformations abnormal shape of the clavicles and ribs calvarial hyperostosis and delayed eruption of permanent teeth. Delayed ambulation is also frequently associated.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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Weismann-Netter syndrome?
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Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
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The Chandler Project brings awareness and shines a light on transformative research surrounding achondroplasia and other skeletal dysplasias by offering support to a global community and network of patients, parents, and caregivers seeking information on scientific discoveries, pharmaceutical advancements and surgical treatment options.
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