Pseudoaminopterin syndrome (Q93991): Difference between revisions
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CID11:ID_893045173 | |||||||||||||||
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15 August 2026
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Latest revision as of 09:06, 16 August 2026
Pseudoaminopterin syndrome is a developmental anomalies syndrome that resembles the aminopterin embryopathy without history of fetal exposure to aminopterin. It is characterised by skull (craniosynostosis and poorly mineralized cranial vault), dysmorphic (ocular hypertelorism, palpebral fissure anomalies, micrognathia cleft lip and/or high arched palate and small and low set/rotated ears) and limb (brachydactyly, syndactyly and clinodactyly) anomalies, associated with mild-to-moderate intellectual deficit and short stature.
| Language | Label | Description | Also known as |
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| default for all languages | ID_893045173 |
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| English | Pseudoaminopterin syndrome |
Pseudoaminopterin syndrome is a developmental anomalies syndrome that resembles the aminopterin embryopathy without history of fetal exposure to aminopterin. It is characterised by skull (craniosynostosis and poorly mineralized cranial vault), dysmorphic (ocular hypertelorism, palpebral fissure anomalies, micrognathia cleft lip and/or high arched palate and small and low set/rotated ears) and limb (brachydactyly, syndactyly and clinodactyly) anomalies, associated with mild-to-moderate intellectual deficit and short stature. |
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CID11:ID_893045173
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dki-india-ID_893045173
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Concluído
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15 August 2026
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