Different Growth Responses to Recombinant Human Growth Hormone in Three Siblings with Isolated Growth Hormone Deficiency Type 1A due to a 6.7Kb Deletion in the GH1 Gene
Isolated growth hormone deficiency (IGHD) type 1A is a rare, autosomal recessive disorder caused by deletion of the GH1 gene and characterized by early onset severe short stature and typical phenotype. Lack of exposure to GH during fetal life often leads to formation of anti-GH antibody following ex...
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| Auteurs principaux: | , , , , , |
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| Format: | article |
| Langue: | EN |
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Galenos Yayincilik
2021
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| Accès en ligne: | https://doaj.org/article/083a3bf876a44f999bf8ba1ffdfca02d |
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