Congenital Hyperinsulinism due to a Compound Heterozygous ABCC8 Mutation with Spontaneous Resolution at Eight Weeks

Publisher： Karger

E-ISSN： 1663-2826|73|4|287-292

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.73, Iss.4, 2010-03, pp. : 287-292

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Familial Glucocorticoid Deficiency Type 1 due to a Novel Compound Heterozygous MC2R Mutation

By  

Hormone Research in Paediatrics, Vol. 69, Iss. 6, 2008-03 ,pp. : 363-368

Karger

Access to resources Recommend Favorite

Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene

By  

Hormone Research in Paediatrics, Vol. 80, Iss. 4, 2013-09 ,pp. : 299-303

Karger

Access to resources Recommend Favorite

Long-Term Follow-Up and Mutation Analysis of 27 Chinese Cases of Congenital Hyperinsulinism

By  

Hormone Research in Paediatrics, Vol. 81, Iss. 3, 2014-01 ,pp. : 169-176

Karger

Access to resources Recommend Favorite

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

By  

Hormone Research in Paediatrics, Vol. 85, Iss. 6, 2016-05 ,pp. : 421-425

Karger

Access to resources Recommend Favorite

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

By  

Hormone Research in Paediatrics, Vol. 85, Iss. 6, 2016-05 ,pp. : 426-427

Karger

Access to resources Recommend Favorite