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spondyloepimetaphyseal dysplasia, Bieganski type

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Spondyloepimetaphyseal dysplasia, Bieganski type is a rare primary bone dysplasia disorder characterized by infantile-onset, progressive, multiple skeletal deformities in association with slowly progressive central and peripheral neurodegeneration. Patients present short stature, coarse facies, psychomotor regression and cognitive impairment. Imaging shows abnormally-shaped vertebral bodies, small, flat epiphyses, and widened metaphyses, as well as cerebral and cerebellar atrophy and progressive axonal-hypomyelinating neuropathy.
Mondo Term and Equivalent IDs
MONDO:0010275:  spondyloepimetaphyseal dysplasia, Bieganski type
GARD:0004891: 
MESH:C536671: 
MESH:C567065: 
UMLS:C1846148: