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

Infantile mitochondrial disorder associated with subclinical hypothyroidism is caused by a rare mitochondrial DNA 8691A>G mutation: a case report.

Neuroreport - 8 Jul 2015

Hao Xiaosheng, Liu Songyan, Wu Xuemei, Hao Yunpeng, Chen Yinbo

Abstract excerpt

Mitochondrial diseases, ~15% of cases, are because of mitochondrial DNA mutations. This study reported a case of an 11-month-old male infant with mitochondrial disease characteristics and subclinical hypothyroidism (a high thyrotropin level). Laboratory tests were all normal and the enzymatic activities of mitochondrial respiratory chain enzyme complexes I-IV were normal. However, thyroid tests showed abnormal...

Read the complete abstract on PubMed

Topics

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

Share to DNA, Mitochondrial
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hypothyroidism

Share to Infant

Share to Magnetic Resonance Imaging

Share to Mitochondrial Diseases

Share to Mitochondrial Proton-Translocating ATPases

Share to Mutation

Source

Identifiers

PMID: 26053701
DOI: 10.1097/WNR.0000000000000392

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Infantile mitochondrial disorder associated with subclinical hypothyroidism is caused by a rare mitochondrial DNA 8691A>G mutation: a case report.PMID 26053701Read ↗

Neurologic disorders due to mitochondrial DNA mutations.Semantic proximity Read ↗

Mitochondrial diseases.Semantic proximity Read ↗

Infantile mitochondrial disorders.Semantic proximity Read ↗

Phenotype-Genotype Analysis Based on Molecular Classification in 135 Children With Mitochondrial Disease.Semantic proximity Read ↗

Mitochondrial disorders.Semantic proximity Read ↗

[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].Semantic proximity Read ↗

The mitochondrial DNA variant m.9032T > C in MT-ATP6 encoding p.(Leu169Pro) causes a complex mitochondrial neurological syndrome.Semantic proximity Read ↗

Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort.Semantic proximity Read ↗

Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA.Semantic proximity Read ↗

A juvenile case of MELAS with T3271C mitochondrial DNA mutation.Semantic proximity Read ↗

A systematic review on the biochemical threshold of mitochondrial genetic variants.Semantic proximity Read ↗

Hypoparathyroidism, neutropenia and nephrotic syndrome in a patient with mitochondrial trifunctional protein deficiency: A case report and review of the literature.Semantic proximity Read ↗

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