Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.

BMC nephrology - 2 May 2023

Xu Jing, He Juan, Xu Shujing, Wang Rui, Peng Nianchun, Zhang Miao

Abstract excerpt

A 14-year-old male patient who suffered from limb numbness, fatigue, and hypokalemia was considered Graves' disease (GD) complicated with thyrotoxic periodic paralysis (TPP) at the first diagnosis. Although with the treatment of antithyroid drugs, he developed severe hypokalemia and rhabdomyolysis (RM). Further laboratory tests revealed hypomagnesemia, hypocalciuria, metabolic alkalosis, hyperrenin, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Gitelman Syndrome
Share to Graves Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypokalemia

Share to Mothers

Share to Mutation

Share to Rhabdomyolysis

Share to Solute Carrier Family 12, Member 3

Source

Open in PubMed Open full text

Identifiers

PMID: 37131142
DOI: 10.1186/s12882-023-03180-8
PMCID: PMC10152583

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.PMID 37131142Read ↗

A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature.Semantic proximity Read ↗

[A case of Gitelman's syndrome presenting with the hypokalemic periodic paralysis].Semantic proximity Read ↗

Gitelman's syndrome with mental retardation.Semantic proximity Read ↗

A rare case of Gitelman's syndrome presenting with hypocalcemia and osteopenia.Semantic proximity Read ↗

[A case of Gitelman syndrome with physical retardation].Semantic proximity Read ↗

Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report.Semantic proximity Read ↗

Gitelman's syndrome: a pathophysiological and clinical update.Semantic proximity Read ↗

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.Semantic proximity Read ↗

A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review.Semantic proximity Read ↗

Gitelman syndrome with primary hyperparathyroidism: A case report.Semantic proximity Read ↗

[Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome].Semantic proximity Read ↗

A NOVEL COMPOUND HETEROZYGOUS VARIANT OF SLC12A3 GENE IN A PEDIGREE WITH GITELMAN SYNDROME CO-EXISTENT WITH THYROID DYSFUNCTION.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.