Literature DB >> 874665

Familial nephrosis, nerve deafness, and hypoparathyroidism.

A Y Barakat, J B D'Albora, M M Martin, P A Jose.   

Abstract

Two male siblings with nephrotic syndrome, nerve deafness, and hypoparathyroidism are described. Each child, one at five years of age and the other at eight years, died in renal failure. At autopsy the parathyroid glands were absent in one child and hypoplastic in the other one. Two twin male siblings presented with similar findings and died at the age of three years. At autopsy their parathyroid glands were fibrotic, and glomerular basement membranes were thickened. This may be the first recorded association of familial nephrosis, nerve deafness, and hypoparathyroidism. The mode of transmission is compatible with autosomal recessive inheritance.

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Year:  1977        PMID: 874665     DOI: 10.1016/s0022-3476(77)80445-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  23 in total

1.  Defective growth hormone secretion and hypogonadism in the new syndrome of congenital hypoparathyroidism, growth failure and dysmorphic features.

Authors:  A T Soliman; A Darwish; I alSalmi; M Asfour
Journal:  Indian J Pediatr       Date:  1996 Sep-Oct       Impact factor: 1.967

Review 2.  Genetics of endocrine and metabolic disorders: parathyroid.

Authors:  R V Thakker
Journal:  Rev Endocr Metab Disord       Date:  2004-03       Impact factor: 6.514

3.  Vitamin D deficiency in a patient with HDR syndrome.

Authors:  Ifigenia Kostoglou-Athanassiou; Dimitrios Stefanopoulos; Areti Karfi; Panagiotis Athanassiou
Journal:  BMJ Case Rep       Date:  2015-07-08

Review 4.  Genetics of vesicoureteral reflux.

Authors:  Prem Puri; Jan-Hendrik Gosemann; John Darlow; David E Barton
Journal:  Nat Rev Urol       Date:  2011-08-23       Impact factor: 14.432

5.  A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.

Authors:  B D Edwards; M A Patton; S A Dilly; J B Eastwood
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

6.  Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease.

Authors:  R Hameed; F Raafat; P Ramani; G Gray; H P Roper; D V Milford
Journal:  Postgrad Med J       Date:  2001-08       Impact factor: 2.401

7.  A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Authors:  S A Sanjad; N A Sakati; Y K Abu-Osba; R Kaddoura; R D Milner
Journal:  Arch Dis Child       Date:  1991-02       Impact factor: 3.791

8.  Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.

Authors:  N J Shaw; D Haigh; G T Lealmann; G Karbani; J T Brocklebank; M J Dillon
Journal:  Arch Dis Child       Date:  1991-10       Impact factor: 3.791

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

Authors:  Amar Al-Shibli; Ibrahim Al Attrach; Patrick J Willems
Journal:  Pediatr Nephrol       Date:  2011-03-12       Impact factor: 3.714

10.  Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.

Authors:  A G Hunter; H Heick; W J Poznanski; P N McLaine
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

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