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

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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Autores principales: Sayan Ghosh, Partha Pratim Chakraborty, Biswabandhu Bankura, Animesh Maiti, Rajkrishna Biswas, Madhusudan Das
Formato: article
Lenguaje:EN
Publicado: Galenos Yayincilik 2021
Materias:
isolated growth hormone deficiency type 1a
gh1 gene
anti-growth hormone antibody
Pediatrics
RJ1-570
Diseases of the endocrine glands. Clinical endocrinology
RC648-665
Acceso en línea:https://doaj.org/article/083a3bf876a44f999bf8ba1ffdfca02d
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https://doaj.org/article/083a3bf876a44f999bf8ba1ffdfca02d

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