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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1643548765 / rank | |||||||||||||||
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CID11:ID_1643548765 | |||||||||||||||
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dki-india-ID_1643548765 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1643548765 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest 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. |
Statements
CID11:ID_1643548765
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dki-india-ID_1643548765
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Concluído
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13 August 2026
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