LEOPARD syndrome (Q53691): Difference between revisions
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Latest revision as of 01:15, 14 August 2026
LEOPARD syndrome is a rare multiple congenital anomalies condition, mainly characterised by skin, facial and cardiac anomalies. LEOPARD is an acronym for the major features of this disorder, including multiple Lentigines, ECG conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and sensorineural Deafness.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_939197023 |
||
| English | LEOPARD syndrome |
LEOPARD syndrome is a rare multiple congenital anomalies condition, mainly characterised by skin, facial and cardiac anomalies. LEOPARD is an acronym for the major features of this disorder, including multiple Lentigines, ECG conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and sensorineural Deafness. |
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CID11:ID_939197023
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dki-india-ID_939197023
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Concluído
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13 August 2026
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