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Chromosome 16p12.2-P11.2 Deletion Syndrome
A chromosomal deletion syndrome that is caused by a chromosome 16p12.2-p11.2 deletion and that is characterized by dysmorphic facial features, feeding difficulties, recurrent ear infections, developmental delay, and cogn
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When to seek help
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Overview
A chromosomal deletion syndrome that is caused by a chromosome 16p12.2-p11.2 deletion and that is characterized by dysmorphic facial features, feeding difficulties, recurrent ear infections, developmental delay, and cogn
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.