15q24 microdeletion syndrome
Name: |
15q24 microdeletion syndrome
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Description: |
15q24 microdeletion syndrome is a rare chromosomal anomaly characterized 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.
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ORPHAcode: |
94065
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Synonyms: |
Del(15)(q24)
Monosomy 15q24
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
01 May 2022 - 06:55
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