Isolated Hypomethylation of IGF2 Associated with Severe Hypoglycemia Responsive to Growth Hormone Treatment

Hypomethylation of H19 and IGF2 can cause Silver–Russell syndrome (SRS), a clinically and genetically heterogeneous condition characterized by intrauterine growth restriction, poor postnatal growth, relative macrocephaly, craniofacial abnormalities, body asymmetry, hypoglycemia and feeding difficult...

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Detalles Bibliográficos
Autores principales: Grünert, Sarah C., Matysiak, Uta, Hodde, Franka, Ruzaike, Gunda, Lausch, Ekkehart, Schumann, Anke, van der Werf-Grohmann, Natascha, Spiekerkoetter, Ute, Schmidts, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146043/
https://www.ncbi.nlm.nih.gov/pubmed/33922271
http://dx.doi.org/10.3390/diagnostics11050749

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146043/
https://www.ncbi.nlm.nih.gov/pubmed/33922271
http://dx.doi.org/10.3390/diagnostics11050749

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