Literature DB >> 7499943

Hearing impairment in association with distal renal tubular acidosis among Saudi children.

S M Zakzouk1, S H Sobki, F Mansour, F H al Anazy.   

Abstract

A follow-up of seven patients with the autosomal recessive inherited syndrome of distal renal tubular acidosis (RTA) and sensorineural hearing loss is described. Five patients were diagnosed as having primary distal renal tubular acidosis and rickets, four were found to have severe sensorineural hearing loss of over 80 dB: two of which are brothers. Two patients were diagnosed as having secondary distal renal acidosis due to a genetic disorder called osteopetrosis; they are brothers and their audiograms showed a mild conductive hearing loss of an average 35 dB bilaterally. All patients had growth retardation with improvement due to alkaline therapy but their hearing loss was not affected by the medication. The pedigrees of two families with half sibs showed the familial incidence for consanguineous marriage. Consanguinity was found to be positive in five out of the seven patients. The tribal tradition in Saudi Arabia fosters consanguineous marriages for cultural and social reasons and pre-arranged marriages are still seen.

Entities:  

Mesh:

Year:  1995        PMID: 7499943     DOI: 10.1017/s0022215100131706

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  8 in total

1.  Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.

Authors:  F E Karet; K E Finberg; A Nayir; A Bakkaloglu; S Ozen; S A Hulton; S A Sanjad; E A Al-Sabban; J F Medina; R P Lifton
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  Carbonic anhydrase II deficiency: report of a novel mutation.

Authors:  Aynaa Alsharidi; Mohammad Al-Hamed; Abdulkareem Alsuwaida
Journal:  CEN Case Rep       Date:  2015-12-08

3.  Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.

Authors:  E H Stover; K J Borthwick; C Bavalia; N Eady; D M Fritz; N Rungroj; A B S Giersch; C C Morton; P R Axon; I Akil; E A Al-Sabban; D M Baguley; S Bianca; A Bakkaloglu; Z Bircan; D Chauveau; M-J Clermont; A Guala; S A Hulton; H Kroes; G Li Volti; S Mir; H Mocan; A Nayir; S Ozen; J Rodriguez Soriano; S A Sanjad; V Tasic; C M Taylor; R Topaloglu; A N Smith; F E Karet
Journal:  J Med Genet       Date:  2002-11       Impact factor: 6.318

4.  Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children.

Authors:  Helena Gil; Fernando Santos; Enrique García; María Victoria Alvarez; Flor A Ordóñez; Serafín Málaga; Eliecer Coto
Journal:  Pediatr Nephrol       Date:  2007-01-11       Impact factor: 3.714

Review 5.  Pediatric renal diseases in the Kingdom of Saudi Arabia.

Authors:  Jameela Abdulaziz Kari
Journal:  World J Pediatr       Date:  2012-08-12       Impact factor: 2.764

Review 6.  Physiological and metabolic implications of V-ATPase isoforms in the kidney.

Authors:  Fiona E Karet
Journal:  J Bioenerg Biomembr       Date:  2005-12       Impact factor: 3.853

7.  Importance of early audiologic assessment in distal renal tubular acidosis.

Authors:  Anand P Swayamprakasam; Elizabeth Stover; Elizabeth Norgett; Katherine G Blake-Palmer; Michael J Cunningham; Fiona E Karet
Journal:  Int Med Case Rep J       Date:  2010-12-22

8.  Carbonic Anhydrase II Deficiency: A Rare Case of Severe Obstructive Sleep Apnea.

Authors:  Emanuela di Palmo; Marcella Gallucci; Elena Tronconi; Rosalba Bergamaschi; Salvatore Cazzato; Claudio La Scola; Giampaolo Ricci; Andrea Pession
Journal:  Front Pediatr       Date:  2018-07-31       Impact factor: 3.418

  8 in total

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