Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report

Isolated growth hormone (GH) deficiency (IGHD) type 2 is a rare autosomal dominant disorder characterized by severe short stature with low GH level. Timely diagnosis is important for optimal results of recombinant human GH (rhGH) treatment and detection of additional pituitary deficiencies in affect...

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Bibliographic Details
Main Authors: Ahmad Kautsar (Author), Jan M. Wit (Author), Aman Pulungan (Author)
Format: Book
Published: Galenos Yayincilik, 2019-12-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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