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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Detalles Bibliográficos
Autores principales: Ghosh, Sayan, Chakraborty, Partha Pratim, Bankura, Biswabandhu, Maiti, Animesh, Biswas, Rajkrishna, Das, Madhusudan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638633/
https://www.ncbi.nlm.nih.gov/pubmed/32936763
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638633/
https://www.ncbi.nlm.nih.gov/pubmed/32936763
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0005

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