Belgian Genetic Tests database
Frank-Ter Haar syndrome
| Name: |
Frank-Ter Haar syndrome
|
| Description: |
A rare primary bone dysplasia characterized by 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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| ORPHAcode: |
137834
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| Synonyms: |
Ter Haar syndrome
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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