Frank-ter Haar syndrome (Q54808): Difference between revisions
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Revision as of 02:26, 14 August 2026
Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles syndrome) is defined by the association of megalocornea, multiple skeletal anomalies, characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism, prominent eyes, full cheeks and micrognathia) and developmental delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1643548765 |
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| English | Frank-ter Haar syndrome |
Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles syndrome) is defined by the association of megalocornea, multiple skeletal anomalies, characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism, prominent eyes, full cheeks and micrognathia) and developmental delay. |
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CID11:ID_1643548765
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dki-india-ID_1643548765
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