Frank-ter Haar syndrome (Q54808): Difference between revisions
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Síndrome de Frank-ter Haar (anteriormente considerada uma forma autossômica recessiva da síndrome de Melnick-Needles) é definida pela associação de megalocórnea, múltiplas anomalias esqueléticas, dismorfismo facial característico (fontanelas largas, testa proeminente, hipertelorismo, olhos proeminentes, bochechas cheias e micrognatia) e atraso no desenvolvimento. | |||
| description / en | description / en | ||
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. | |||
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. |
