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11q partial monosomy syndrome

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Description

Jacobsen syndrome (JBS) is a contiguous gene deletion syndrome with major clinical features of growth retardation, psychomotor retardation, trigonocephaly, divergent intermittent strabismus, epicanthus, telecanthus, broad nasal bridge, short nose with anteverted nostrils, carp-shaped upper lip, retrognathia, low-set dysmorphic ears, bilateral camptodactyly, hammertoes, and isoimmune thrombocytopenia (Fryns et al., 1986, Epstein, 1986).

OMIM

  • Mode of Inheritance

  • Sporadic

VARIANTS

1

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Genes

    External Links

    • OMIM

      147791

    • Orphanet

      2308

    • HPO
    • Medgen

      C0795841

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