Dermatological Manifestations of Wilson’s Disease: Two Cases

Authors

  • Rubaiyat Alam Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University, Dhaka
  • ASM Bazlul Karim Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University, Dhaka
  • Md Rukunuzzaman Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University, Dhaka
  • Kamal Hossen Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University, Dhaka
  • Shashi Bhushan Thakur Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University, Dhaka
  • Mohammad Moin Uddin Department of Physical Medicine, Chittagong Medical College, Chittagong

DOI:

https://doi.org/10.3329/cmoshmcj.v16i2.37299

Keywords:

Skin lesions, Wilson’s disease, Copper matabolism

Abstract

Wilson's disease, an autosomal recessive disorder of copper metabolism, most commonly presents either with hepatic or neurological features. But it may sometimes have certain atypical presentations which may lead to diagnostic difficulties. We report here two cases who were diagnosed as Wilson's disease with prominent skin lesions over both lower extremities. These cases are reported here as it is rare and to highlight the fact that early recognition of the skin lesions may play a role in the diagnosis of Wilson's disease. The need to highlight the importance of skin lesion as a pointer to the early diagnosis of Wilson's disease because specific treatment can prevent further liver injury and neurological complications in most cases.

Chatt Maa Shi Hosp Med Coll J; Vol.16 (2); July 2017; Page 59-62

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Published

2018-07-03

How to Cite

Alam, R., Karim, A. B., Rukunuzzaman, M., Hossen, K., Thakur, S. B., & Uddin, M. M. (2018). Dermatological Manifestations of Wilson’s Disease: Two Cases. Chattagram Maa-O-Shishu Hospital Medical College Journal, 16(2), 59–62. https://doi.org/10.3329/cmoshmcj.v16i2.37299

Issue

Vol. 16 No. 2 (2017)

Section

Case Reports

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