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A rare case of mucopolysaccharidosis: Hunter syndrome
We report a rare case of Hunter syndrome—mucopolysaccharidosis type II (MPS II) with atypical presentation of mild mental retardation, acrocephalic head without corneal clouding, and multiple skin eruptions along with oral, dental, and radiographic findings. It is a rare syndrome with a very low pre...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3361789/ https://ncbi.nlm.nih.gov/pubmed/22690062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-9668.95984 |
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