Background: Insulin resistance syndromes are a heterogeneous group of disorders with variable clinical phenotypes, associated with increased blood glucose and insulin levels. Case Presentation: Herein, a 10-year old girl with abnormal face and dentition is presented. She has suffered from diabetes mellitus type I since she was 6 years old. Hyperglycemia did not respond to age appropriate insulin dosage; therefore, insulin dosage was increased, but did not lead to appropriate glycemic control. Twenty two exons of insulin receptor gene (INSR), on short arm of chromosome 19, were sequenced, but no identifiable disease causing mutation was detected. Conclusion: Although a rare mutation within the intronic or promoter region has not been exclude...
International audienceMajor hyperinsulinemia, acanthosis nigricans, impaired glucose tolerance and o...
AIM: Hypoglycemia in childhood is very rare and can be caused by genetic mutations or insulin-secret...
This thesis describes the characterization of several mutations found in subjects with severe insuli...
Background Inherited severe insulin resistance syndromes (SIRS) are rare and can be caused by mutati...
Rabson-Mendenhall syndrome (RMS) is an autosomal recessive disorder due to mutations in the insulin ...
Background. Mutations in insulin receptor genes can cause severe insulin resistance syndrome. Compar...
We have identified two sisters (12 and 17 years old) affected by acanthosis nigricans-insulin resis...
Aim: Hypoglycemia in childhood is very rare and can be caused by genetic mutations or insulin-secre...
Biallelic insulin receptor (INSR) gene mutations cause congenital syndromes of severe insulin resist...
Bi-allelic insulin receptor (INSR) gene mutations cause congenital syndromes of severe insulin resis...
OBJECTIVE: Heterozygous, gain-of-function mutations of the insulin gene can cause permanent diabete...
Insulin resistance is frequently associated with acanthosis nigricans and hyperandrogenism. In patie...
Background.Insulin gene (INS) mutations have recently been described as a common cause of permanent ...
Andrey O Emelyanov,1 Elena Sechko,1 Ekaterina Koksharova,1 Igor Sklyanik,1 Tamara Kuraeva,1,2 Alexan...
Mutations of the insulin receptor gene have been identified in patients with genetic syndromes of in...
International audienceMajor hyperinsulinemia, acanthosis nigricans, impaired glucose tolerance and o...
AIM: Hypoglycemia in childhood is very rare and can be caused by genetic mutations or insulin-secret...
This thesis describes the characterization of several mutations found in subjects with severe insuli...
Background Inherited severe insulin resistance syndromes (SIRS) are rare and can be caused by mutati...
Rabson-Mendenhall syndrome (RMS) is an autosomal recessive disorder due to mutations in the insulin ...
Background. Mutations in insulin receptor genes can cause severe insulin resistance syndrome. Compar...
We have identified two sisters (12 and 17 years old) affected by acanthosis nigricans-insulin resis...
Aim: Hypoglycemia in childhood is very rare and can be caused by genetic mutations or insulin-secre...
Biallelic insulin receptor (INSR) gene mutations cause congenital syndromes of severe insulin resist...
Bi-allelic insulin receptor (INSR) gene mutations cause congenital syndromes of severe insulin resis...
OBJECTIVE: Heterozygous, gain-of-function mutations of the insulin gene can cause permanent diabete...
Insulin resistance is frequently associated with acanthosis nigricans and hyperandrogenism. In patie...
Background.Insulin gene (INS) mutations have recently been described as a common cause of permanent ...
Andrey O Emelyanov,1 Elena Sechko,1 Ekaterina Koksharova,1 Igor Sklyanik,1 Tamara Kuraeva,1,2 Alexan...
Mutations of the insulin receptor gene have been identified in patients with genetic syndromes of in...
International audienceMajor hyperinsulinemia, acanthosis nigricans, impaired glucose tolerance and o...
AIM: Hypoglycemia in childhood is very rare and can be caused by genetic mutations or insulin-secret...
This thesis describes the characterization of several mutations found in subjects with severe insuli...