POSSIBILITIES AND LIMITS OF THERAPY IN A CASE OF HYPOCHONDROPLASIA

Hypocondroplasia is an autosomal dominant genetic disease caused by mutations in the receptor 3 of the fi broblast growth factor gene. The short stature's negative impact on quality of life can be improved by early diagnosis and prompt recombinant growth hormone therapy. The authors present the...

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Bibliographic Details
Main Authors: Monica Alexoae (Author), Aurica Rugina (Author), Evelina Moraru (Author), Ileana Ioniuc (Author)
Format: Book
Published: Amaltea Medical Publishing House, 2014-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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