Literature DB >> 18404978

Hypokalemic rhabdomyolysis in a child with 11-hydroxylase deficiency.

Mehmet Emre Atabek1, Ozgur Pirgon, Ahmet Sert.   

Abstract

Myopathy is a well-recognized complication of persistent hypokalemia. Although hypokalemic myopathy may be due to divers diseases or to drug administration, hypokalemic rhabdomyolysis as a complication of under-treated 11-hydroxylase deficiency has not previously been described in the literature. We describe a 10-year-old boy with under-treated 11-hydroxylase deficiency who developed rhabdomyolysis following severe hypokalemia. Patients with under-treated 11-hydroxylase deficiency may present with hypokalemia in association with muscle weakness; if serum potassium is markedly low, rhabdomyolysis may occur. Hypokalemia-induced rhabdomyolysis should be carefully followed.

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Year:  2008        PMID: 18404978     DOI: 10.1515/jpem.2008.21.1.93

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  2 in total

Review 1.  [Change in stature after pseudo-puberty early by 11ß hydroxylase deficiency in a girl of 7 years: report of a case and review of literature].

Authors:  Hanane Latrech; Ahmed Gaouzi
Journal:  Pan Afr Med J       Date:  2015-02-23

2.  A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency.

Authors:  Hong Chen; Ke Yuan; Bingtao Zhang; Zexiao Jia; Chun Chen; Yilin Zhu; Yaping Sun; Hui Zhou; Wendong Huang; Li Liang; Qingfeng Yan; Chunlin Wang
Journal:  Front Genet       Date:  2019-10-22       Impact factor: 4.599

  2 in total

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