Literature DB >> 17657093

Paralysis Episodes in Carbonic Anhydrase II Deficiency.

Alia Al-Ibrahim1, Mosa Al-Harbi, Sulaiman Al-Musallam.   

Abstract

Carbonic anhydrase II (CAII) deficiency is an autosomal recessive disorder manifest by osteopetrosis, renal tubular acidosis, and cerebral calcification. Other features include growth failure and mental retardation. Complications of the osteopetrosis include frequent bone fractures, cranial nerve compression, and dental mal-occlusion. A hyper-chloremic metabolic acidosis, sometimes with hypokalemia, occurs due to renal tubular acidosis that may be proximal, distal, or more commonly, the combined type. Such patients may present with global hypotonia, muscle weakness or paralysis. We report a case of CA II deficiency with recurrent attacks of acute paralysis which was misdiagnosed initially as Guillian-Barre syndrome.

Entities:  

Year:  2003        PMID: 17657093

Source DB:  PubMed          Journal:  Saudi J Kidney Dis Transpl        ISSN: 1319-2442


  3 in total

1.  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

2.  A novel homozygous nonsense mutation in the CA2 gene (c.368G>A, p.W123X) linked to carbonic anhydrase II deficiency syndrome in a Chinese family.

Authors:  Yan Yang; Nie Tang; Ying Zhu; Lei Zhang; Xu Cao; Limei Liu; Wei Xia; Pengqiu Li; Yi Yang
Journal:  Metab Brain Dis       Date:  2021-02-08       Impact factor: 3.584

3.  Carbonic Anhydrase II Deficiency in a Saudi Woman.

Authors:  Omar N Alhuzaim; Ohoud M Almohareb; Safiya M Sherbeeni
Journal:  Clin Med Insights Case Rep       Date:  2015-02-03
  3 in total

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