Weissenbacher- Zweymuller syndrome

Weissenbacher-Zweymuller syndrome (WZS) is characterized by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.

Metaphyseal widening

Abnormal widening of the metaphyseal regions of long bones.


合計: 1

                       


（表示件数）
PMID (PMCID)
1415350
 MIXED_SAMPLE Child
Weissenbacher-Zweymuller syndrome: a distinct autosomal recessive skeletal dysplasia.
Chemke J, Carmi R, Galil A, Bar-Ziv Y, Ben-Ytzhak I, Zurkowski L.
Am J Med Genet. 1992;43(6):989-95.
The Weissenbacher-Zweymuller syndrome (WZS) is defined as congenital neonatal rhizomelic dwarfism with metaphyseal widening of the long bones and vertebral coronal clefts.