15q24 deletion (Q101705): Difference between revisions
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A síndrome de microdeleção 15q24 é uma síndrome rara recentemente descrita, caracterizada citogeneticamente por uma deleção de 1,7-6,1 Mb no cromossomo 15q24 e clinicamente por retardo de crescimento pré e pós-natal, incapacidade intelectual, características faciais distintas e anomalias genitais, esqueléticas e digitais. | |||
| description / en | description / en | ||
15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies. | |||
Revision as of 18:32, 16 August 2026
15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1382727392 |
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| English | 15q24 deletion |
15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies. |
