Diaphanospondylodysostosis (Q86536): Difference between revisions

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Diáfano-espôndilo-disostose é uma displasia esquelética caracterizada por ossificação ausente dos corpos vertebrais e do sacro associada a anomalias variáveis (pescoço curto, tórax curto e largo, número reduzido de costelas, pelve estreita e anomalias inconstantes, como mielomeningocele, rins císticos com resquícios nefrogênicos e fenda palatina).
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Diaphanospondylodysostosis is a skeletal dysplasia characterised by absent ossification of the vertebral bodies and sacrum associated with variable anomalies (short neck, a short wide thorax, a reduced number of ribs, a narrow pelvis, and inconstant anomalies such as myelomeningocele, cystic kidneys with nephrogenic rests, and cleft palate).

Revision as of 11:57, 15 August 2026

Diaphanospondylodysostosis is a skeletal dysplasia characterised by absent ossification of the vertebral bodies and sacrum associated with variable anomalies (short neck, a short wide thorax, a reduced number of ribs, a narrow pelvis, and inconstant anomalies such as myelomeningocele, cystic kidneys with nephrogenic rests, and cleft palate).
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ID_508093071
    English
    Diaphanospondylodysostosis
    Diaphanospondylodysostosis is a skeletal dysplasia characterised by absent ossification of the vertebral bodies and sacrum associated with variable anomalies (short neck, a short wide thorax, a reduced number of ribs, a narrow pelvis, and inconstant anomalies such as myelomeningocele, cystic kidneys with nephrogenic rests, and cleft palate).

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