Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.
case_report · Level V
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- Record sourced from PubMed, PMID 1719942.
- Also identified by PMC identifier 1793490.
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Abstract
Four children (two boys and two girls) with hypoparathyroidism, renal insufficiency, and developmental delay are described. They were the products of consanguineous marriages in three related Asian families presenting over a six year period. All the children died within the first 15 months of life despite treatment. Postmortem examination on one child showed absent parathyroid glands. We believe these children represent a previously undescribed syndrome that appears to be inherited in an autosomal recessive manner.
Medical subject headings
- Developmental Disabilities
- Genes, Recessive
- Hypoparathyroidism
- Kidney Failure, Chronic