McDonough syndrome (Q94183): Difference between revisions
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Revision as of 09:18, 16 August 2026
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1349711155 |
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| English | McDonough syndrome |
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect. |
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CID11:ID_1349711155
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dki-india-ID_1349711155
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