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

L. I. Al-Gazali; A. Dawodu

doi:10.1097/00019605-199707000-00006

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

L. I. Al-Gazali, A. Dawodu

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	233-237
Number of pages	5
Journal	Clinical Dysmorphology
Volume	6
Issue number	3
DOIs	https://doi.org/10.1097/00019605-199707000-00006
Publication status	Published - 1997

Keywords

Arabs
Autosomal recessive
Developmental delay
Hypoparathyroidism

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Anatomy
Pathology and Forensic Medicine
Genetics(clinical)

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10.1097/00019605-199707000-00006

Cite this

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

Abstract

Keywords

ASJC Scopus subject areas

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