Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2007.02203.x/fullpdf
Reference22 articles.
1. Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families
2. Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II
3. The effect of haematopoietic stem cell transplant on papules with 'pebbly' appearance in Hunter's syndrome
4. Extensive Mongolian spots associated with Hunter syndrome
5. Extensive Mongolian Spots in an Infant With Hurler Syndrome
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3. A Case of Mucopolysaccharidosis II Caused by a Novel Variant with Skin Linear Hyperpigmented Streaks along Blaschko’s Lines;International Journal of Molecular Sciences;2023-03-15
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