Hunter Syndrome: Clinical Case of Early Diagnostics

Background. This clinical case of orphan disease can be interesting for its early diagnostics which is essential for timely specific therapy and sufficient dynamic observation. Clinical case description. Mucopolysaccharidosis type II (Hunter syndrome) diagnosis at the age of 12 months was based on c...

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Bibliographic Details
Main Authors: Natalya N. Martynovich (Author), Yulia P. Semshchikova (Author), Natalya Yu. Rudenko (Author), Vera M. Shinkareva (Author), Kristina V. Egorycheva (Author)
Format: Book
Published: Union of pediatricians of Russia, 2020-11-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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