The Effect of Combined Growth Hormone and a Gonadotropin-Releasing Hormone Agonist Therapy on Height in Korean 3-M Syndrome Siblings

3-M syndrome is a rare autosomal recessive growth disorder characterized by severe growth retardation, low birth weight, characteristic facial features, and skeletal anomalies, for which three causative genes (CUL7, OBSL1, and CCDC8) have been identified. We herein report two Korean siblings with 3-...

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Detalles Bibliográficos
Autores principales: Lee, In Kyung, Lim, Han Hyuk, Kim, Yoo-Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593105/
https://www.ncbi.nlm.nih.gov/pubmed/33107243
http://dx.doi.org/10.3349/ymj.2020.61.11.981

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593105/
https://www.ncbi.nlm.nih.gov/pubmed/33107243
http://dx.doi.org/10.3349/ymj.2020.61.11.981

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