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| Content Provider | frontiers |
|---|---|
| Author | Zou, Ju Wang, Ying-Hao Wang, Ling Chen, Ruo-Chan |
| Description | Abstract: Background: Wilson’s disease (WD) is a rare condition whose diagnosis is challenging due to a wide spectrum of ATP7B genotypes and variable clinical phenotypes, along with environmental factors. Few cases of WD with presentation of skin lesions and acute neurovisceral symptoms have been reported in the literature. To our knowledge, this is the first reported case of WD with an uncommon ATP7B gene mutation and rare symptoms of photosensitivity, sensation abnormality and skin eruption occurring in a 19-year-old woman. Case presentation: We report the case of a 19-year-old woman with WD presenting with liver failure, skin manifestations and acute neurovisceral symptoms .The rare mutation in intron 1 of ATP7B [c.51+2T>G] was further confirmed by gene sequencing. The patient recovered after administration of penicillamine and zinc therapy combined with plasma exchange. She received long-term penicillamine treatment, and her liver function was within the normal range at the latest follow-up (1 year after discharge). Conclusions: We present a case of WD with a novel ATP7B gene mutation that may serve as a reference to generalists and specialists in hepatology or neurology of the rare clinical characteristics of WD, to prevent misdiagnosis and aid in the early diagnosis and treatment of the condition. |
| Abstract | Background: Wilson's disease (WD) is a rare condition; its diagnosis is challenging owing to a wide spectrum of ATP7B genotypes and variable clinical phenotypes, along with environmental factors. Few cases of WD with presentation of skin lesions and acute neurovisceral symptoms have been reported in the literature. To our knowledge, this is the first reported case of WD with an uncommon ATP7B gene mutation and rare symptoms of photosensitivity, sensation abnormality, and skin eruption occurring in a 19-year-old woman.Case presentation: We report the case of a 19-year-old woman with WD presenting with liver failure, skin manifestations, and acute neurovisceral symptoms.The rare mutation in intron 1 of ATP7B (c.51+2T > G) was further confirmed by gene sequencing. The patients' symptoms improved after administration of penicillamine and zinc therapy combined with plasma exchange. She received long-term penicillamine treatment, and her liver function was within the normal range at 1 year after discharge. However, she underwent liver transplantation at 1.5 years after discharge.Conclusions: We present a case of WD with a novel ATP7B gene mutation that may serve as a reference to generalists and specialists in hepatology or neurology of the rare clinical characteristics of WD, to prevent misdiagnosis and aid in the early diagnosis and treatment of the condition. |
| ISSN | 2296858X |
| DOI | 10.3389/fmed.2021.702312 |
| Volume Number | 8 |
| Journal | Frontiers in Medicine |
| Language | English |
| Publisher Date | 2021-07-26 |
| Access Restriction | Open |
| Subject Keyword | Copper storage disease ATP7B Liver Failure Wilson'sdisease Porphyria |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine |
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