Pseudo-dominant Wilson disease with an unresolved third-generation ATP7B finding

Wilson disease is an autosomal recessive copper metabolism disorder caused by pathogenic variants in the adenosine triphosphatase (ATPase) copper transporting beta gene (ATP7B ). We describe a Han Chinese family from Inner Mongolia with genetically confirmed pseudo-dominant Wilson disease in two consecutive generations and an unresolved diagnosis in a third-generation relative. Whole-exome sequencing and Sanger segregation analysis showed that the proband carried c.2621C>T (p.Ala874Val) and c.2333G>T (p.Arg778Leu) in trans. Her son and daughter carried c.2621C>T (p.Ala874Val) and c.2975C>T (p.Pro992Leu); their trans configuration and paternal origin of p.Pro992Leu were inferred from the pedigree because the deceased father was unavailable for testing. The 22-year-old grandson had a previous clinical diagnosis but only monoallelic c.2621C>T, negative Kayser-Fleischer rings, and no second ATP7B variant detected by whole-exome sequencing. This family highlights the need for careful phase assignment, spouse and offspring screening, and cautious reconciliation of clinical and molecular diagnoses.

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Publication Details

Journal
Rare Disease and Orphan Drugs Journal
Published
2026-10-26
DOI
https://doi.org/10.20517/rdodj.2026.46
Primary Topic
Trace Elements in Health
Type
article
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article

Pseudo-dominant Wilson disease with an unresolved third-generation ATP7B finding

Sujun Zheng, 支建平, Wei Hou, Zhili Yuan et al.
Rare Disease and Orphan Drugs Journal
Trace Elements in Health
article

Pseudo-dominant Wilson disease with an unresolved third-generation ATP7B finding

Sujun Zheng, 支建平, Wei Hou, Zhili Yuan, Wenjuan Mi
article en

Abstract

Wilson disease is an autosomal recessive copper metabolism disorder caused by pathogenic variants in the adenosine triphosphatase (ATPase) copper transporting beta gene (ATP7B ). We describe a Han Chinese family from Inner Mongolia with genetically confirmed pseudo-dominant Wilson disease in two consecutive generations and an unresolved diagnosis in a third-generation relative. Whole-exome sequencing and Sanger segregation analysis showed that the proband carried c.2621C>T (p.Ala874Val) and c.2333G>T (p.Arg778Leu) in trans. Her son and daughter carried c.2621C>T (p.Ala874Val) and c.2975C>T (p.Pro992Leu); their trans configuration and paternal origin of p.Pro992Leu were inferred from the pedigree because the deceased father was unavailable for testing. The 22-year-old grandson had a previous clinical diagnosis but only monoallelic c.2621C>T, negative Kayser-Fleischer rings, and no second ATP7B variant detected by whole-exome sequencing. This family highlights the need for careful phase assignment, spouse and offspring screening, and cautious reconciliation of clinical and molecular diagnoses.

Rare Disease and Orphan Drugs JournalVol. 5(4)
Capital Medical University (CN), Second Affiliated Hospital of Inner Mongolia Medical University (CN), Beijing YouAn Hospital (CN), Hohhot First Hospital (CN), Fourth Hospital of Inner Mongolia (CN)
Openalex Percentile: Top 13%
Trace Elements in Health
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Pseudo-dominant Wilson disease with an unresolved third-generation ATP7B finding — Sujun Zheng, 支建平, et al. · Rare Disease and Orphan Drugs Journal (2026) | TGRS Research Map | TGRS