Abstract
We report a 10-years-old female patient with a partial trisomy 18q and monosomy 11q due to a maternal translocation. The phenotype of our proband is partially common with Jacobsen syndrome and duplication 18q but she has also some atypical anomalies such as precocious puberty, a retinal albinism and hypermetropia. Based on cytogenetics and FISH analysis, the karyotype of the proband was 46,XX,der(11)t(11;18)(q24;q13). To the best of our knowledge, this is the first report of precocious puberty associated with either dup(18q) or del(11q) syndromes.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Abnormalities, Multiple / diagnosis
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Abnormalities, Multiple / genetics*
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Child
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Child, Preschool
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Chromosomes, Human, Pair 11 / genetics*
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Chromosomes, Human, Pair 18 / genetics*
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Craniofacial Abnormalities / diagnosis
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Craniofacial Abnormalities / genetics*
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Developmental Disabilities / diagnosis
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Developmental Disabilities / genetics*
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Facies
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Female
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Follow-Up Studies
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Genetic Carrier Screening
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Humans
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In Situ Hybridization, Fluorescence
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Karyotyping
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Monosomy / genetics*
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Puberty, Precocious / genetics*
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Translocation, Genetic / genetics
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Trisomy / genetics*