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Article

The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies.

Clinical dysmorphology - 1 Jul 1997

al-Gazali L I, Dawodu A

Abstract excerpt

We report a child from a highly inbred Omani family with hypoparathyroidism, growth failure, developmental delay and a distinctive facial appearance. Thirty cases with this syndrome have been previously reported; 22 came from the Arab Gulf Countries and eight were Arabs living in Israel. These cases are reviewed.

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PMID: 9220193
DOI: 10.1097/00019605-199707000-00006

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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