Micro syndrome (Q68285): Difference between revisions
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Síndrome Micro é um transtorno autossômico recessivo caracterizado por defeitos oculares e do neurodesenvolvimento e por microgenitália. Ela se apresenta com incapacidade intelectual grave, microcefalia, catarata congênita, microcórnea, microftalmia, agenesia/hipoplasia do corpo caloso e hipogenitalismo. | |||
| description / en | description / en | ||
Micro syndrome is an autosomal recessive disorder characterised by ocular and neurodevelopmental defects and by microgenitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism. | |||
Revision as of 16:09, 14 August 2026
Micro syndrome is an autosomal recessive disorder characterised by ocular and neurodevelopmental defects and by microgenitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1843090232 |
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| English | Micro syndrome |
Micro syndrome is an autosomal recessive disorder characterised by ocular and neurodevelopmental defects and by microgenitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism. |
