Abstract
A stillborn male infant with a ring chromosome 15 and some features compatible with Fryns' syndrome is presented. Neither diagnosis is common and the overlap may be of significance.
MeSH terms
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Abnormalities, Multiple / genetics*
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Chromosome Aberrations*
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Chromosomes, Human, Pair 15* / ultrastructure
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Female
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Fetal Death
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Humans
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Infant, Newborn
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Karyotyping
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Male
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Pregnancy
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Ring Chromosomes*
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Syndrome