Literature DB >> 1719942

Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.

N J Shaw1, D Haigh, G T Lealmann, G Karbani, J T Brocklebank, M J Dillon.   

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.

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Year:  1991        PMID: 1719942      PMCID: PMC1793490          DOI: 10.1136/adc.66.10.1191

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  10 in total

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Journal:  Arch Dis Child       Date:  1959-08       Impact factor: 3.791

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Journal:  Lancet       Date:  1987-02-07       Impact factor: 79.321

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Authors:  M P Whyte; V V Weldon
Journal:  J Pediatr       Date:  1981-10       Impact factor: 4.406

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Journal:  Arch Dis Child       Date:  1991-02       Impact factor: 3.791

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Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

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Journal:  Arch Dis Child       Date:  1986-07       Impact factor: 3.791

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Journal:  J Pediatr       Date:  1983-09       Impact factor: 4.406

10.  Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy.

Authors:  P J Dahlberg; W Z Borer; K L Newcomer; W R Yutuc
Journal:  Am J Med Genet       Date:  1983-09
  10 in total
  8 in total

Review 1.  Molecular genetics of mineral metabolic disorders.

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Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

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4.  Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia.

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5.  Living-donor kidney transplantation for a patient with hypoparathyroidism, deafness, and renal dysplasia syndrome.

Authors:  Nobutaka Nishimura; Shunta Hori; Chihiro Omori; Makito Miyake; Satoshi Anai; Kazumasa Torimoto; Katsuya Aoki; Nobumichi Tanaka; Tatsuo Yoneda; Kiyohide Fujimoto
Journal:  IJU Case Rep       Date:  2020-07-27

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Authors:  D B Parkinson; N J Shaw; R L Himsworth; R V Thakker
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

7.  Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.

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Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

8.  Seizure, deafness, and renal failure: a case of barakat syndrome.

Authors:  Nasrollah Maleki; Bahman Bashardoust; Manouchehr Iranparvar Alamdari; Zahra Tavosi
Journal:  Case Rep Nephrol       Date:  2013-10-22
  8 in total

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