Mowat-Wilson syndrome (Q94200): Difference between revisions
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15 August 2026
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Latest revision as of 09:19, 16 August 2026
Mowat-Wilson syndrome is a multiple congenital anomaly syndrome characterised by a distinct facial phenotype (high forehead, frontal bossing, large eyebrows, medially flaring and sparse in the middle part, hypertelorism, deep set but large eyes, large and uplifted ear lobes with a central depression, saddle nose with prominent rounded nasal tip, prominent columella, open mouth with M-shaped upper lip, frequent smiling, and a prominent but narrow and triangular pointed chin), moderate-to-severe intellectual deficiency, epilepsy and variable congenital malformations including Hirschsprung disease (HSCR), genitourinary anomalies (in particular hypospadias in males), congenital heart defects, agenesis of the corpus callosum and eye anomalies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1985672762 |
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| English | Mowat-Wilson syndrome |
Mowat-Wilson syndrome is a multiple congenital anomaly syndrome characterised by a distinct facial phenotype (high forehead, frontal bossing, large eyebrows, medially flaring and sparse in the middle part, hypertelorism, deep set but large eyes, large and uplifted ear lobes with a central depression, saddle nose with prominent rounded nasal tip, prominent columella, open mouth with M-shaped upper lip, frequent smiling, and a prominent but narrow and triangular pointed chin), moderate-to-severe intellectual deficiency, epilepsy and variable congenital malformations including Hirschsprung disease (HSCR), genitourinary anomalies (in particular hypospadias in males), congenital heart defects, agenesis of the corpus callosum and eye anomalies. |
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CID11:ID_1985672762
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dki-india-ID_1985672762
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Concluído
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15 August 2026
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