Weissenbacher- Zweymuller syndrome (Q88326): Difference between revisions

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Revision as of 14:31, 15 August 2026

Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.
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ID_1421501711
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    Weissenbacher- Zweymuller syndrome
    Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.

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