ID

45211

Beskrivning

Principal Investigator: Tadafumi Kato, MD, PhD, RIKEN Brain Science Institute, Saitama, Japan MeSH: Ophthalmoplegia, Chronic Progressive External https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000392 Progressive external ophthalmoplegia (PEO) is an inherited mitochondrial disease that follows either autosomal dominant or recessive forms of inheritance (adPEO or arPEO). AdPEO is a genetically heterogeneous disease and several genes including *POLG1* and *C10orf2*/Twinkle have been identified as responsible genes. On the other hand, *POLG1* was the only established gene causing arPEO with mitochondrial DNA deletions. We previously reported a case of PEO with unidentified genetic etiology. The patient was born of a first-cousin marriage. Therefore, the recessive form of inheritance was suspected. To identify the disease causing variant in this patient, we subjected the patient's DNA to whole-exome sequencing and narrowed down the candidate variants using public data and runs of homozygosity analysis.

Länk

dbGaP study = phs000392

Nyckelord

  1. 2022-08-02 2022-08-02 - Simon Heim
  2. 2022-10-12 2022-10-12 - Adrian Schulz
Rättsinnehavare

Tadafumi Kato, MD, PhD, RIKEN Brain Science Institute, Saitama, Japan

Uppladdad den

12 oktober 2022

DOI

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Licens

Creative Commons BY 4.0

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dbGaP phs000392 Exome Sequencing of arPEO

Eligibility Criteria

Inclusion and exclusion criteria
Beskrivning

Inclusion and exclusion criteria

Single case of progressive external ophthalmoplegia was included.
Beskrivning

Single case of progressive external ophthalmoplegia was included.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0162674

Similar models

Eligibility Criteria

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion and exclusion criteria
Single case of progressive external ophthalmoplegia was included.
Item
Single case of progressive external ophthalmoplegia was included.
boolean
C1512693 (UMLS CUI [1,1])
C0162674 (UMLS CUI [1,2])

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