A boy with developmental delay and a maternally inherited deletion in 15q11q13. |
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| Authors: | M King C Hardy B Asenbauer M Kilpatrick T Webb |
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| Affiliation: | Children''s Hospital, Dublin 1, Ireland. |
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| Abstract: | A boy was referred at 8 weeks of age for failure to thrive. Cytogenetic and molecular studies showed that he had a large proximal deletion of the maternally derived chromosome 15q. He did not have Angelman syndrome, but at 2 years of age was severely globally delayed. He died at 2 1/2 years of age. |
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