Holmes-Schepens syndrome (Q94179): Difference between revisions
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Síndrome de Holmes-Schepens, também conhecida como síndrome de Donnai-Barrow, é uma síndrome de malformação caracterizada por hérnia diafragmática, exonfalo, hipertelorismo, agenesia do corpo caloso, surdez neurossensorial grave e miopia grave. | |||
| description / en | description / en | ||
Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia. | |||
Revision as of 09:18, 16 August 2026
Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1171547698 |
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| English | Holmes-Schepens syndrome |
Holmes-Schepens syndrome also known as Donnai-Barrow syndrome is a malformation syndrome characterised by diaphragmatic hernia, exomphalos, hypertelorism, agenesis of the corpus callosum, severe sensorineural deafness, and severe myopia. |
