Upper limb defect associated with developmental delay, unilateral poorly developed antihelix, hearing deficit, and bilateral choroid coloboma: a new syndrome.
case_report · Level V
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- Record sourced from PubMed, PMID 1518028.
- Also identified by PMC identifier 1016070.
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Abstract
Two sibs are reported with upper limb defect, developmental delay, central hearing loss, unilateral poorly developed antihelix, and bilateral choroid coloboma. The inheritance is probably autosomal recessive.
Medical subject headings
- Abnormalities, Multiple
- Arm
- Ear
- Hearing Disorders