scholarly journals Erratum: Advances in the diagnosis and management of hyperinsulinemic hypoglycemia

2009 ◽  
Vol 5 (3) ◽  
pp. 180-180 ◽  
Author(s):  
Ritika R Kapoor ◽  
Chela James ◽  
Khalid Hussain
Keyword(s):  
Hyperinsulinemic Hypoglycemia ◽  
Diagnosis And Management

scholarly journals Hyperinsulinemic Hypoglycemia after Bariatric Surgery: Diagnosis and Management Experience from a Spanish Multicenter Registry

Obesity Facts ◽  
2016 ◽  
Vol 9 (1) ◽  
pp. 41-51 ◽  
Author(s):  
Nuria Vilarrasa ◽  
Albert Goday ◽  
Miguel Angel Rubio ◽  
Assumpta Caixàs ◽  
Silvia Pellitero ◽  
...  
Keyword(s):  
Bariatric Surgery ◽  
Hyperinsulinemic Hypoglycemia ◽  
Diagnosis And Management ◽  
Management Experience ◽  
Multicenter Registry

Diagnosis and Management of Hyperinsulinemic Hypoglycemia

2009 ◽  
pp. 493-506 ◽  
Author(s):  
Adrian Vella ◽  
Geoffrey B. Thompson ◽  
F. John Service
Keyword(s):  
Hyperinsulinemic Hypoglycemia ◽  
Diagnosis And Management

Hyperinsulinemic hypoglycemia in infancy: Current concepts in diagnosis and management

2015 ◽  
Vol 52 (12) ◽  
pp. 1051-1059 ◽  
Author(s):  
Shrenik Vora ◽  
Suresh Chandran ◽  
Victor Samuel Rajadurai ◽  
Khalid Hussain
Keyword(s):  
Hyperinsulinemic Hypoglycemia ◽  
Diagnosis And Management

scholarly journals Hyperinsulinism-hyperammonemia syndrome in an infant with seizures

2018 ◽  
Vol 21 (1) ◽  
pp. 77-81
Author(s):  
A Strajnar ◽  
MZ Tansek ◽  
KT Podkrajsek ◽  
T Battelino ◽  
U Groselj
Keyword(s):  
Genetic Testing ◽  
Brain Injury ◽  
Clinical Characteristics ◽  
Metabolic Disorders ◽  
Autosomal Dominant ◽  
Hyperinsulinemic Hypoglycemia ◽  
Neurological Development ◽  
Subsequent Growth ◽  
Diagnosis And Management ◽  
Timely Diagnosis

Abstract Hyperinsulinism-hyperammonemia syndrome (HI/HA) is the second most common form of persistent hyperinsulinemic hypoglycemia of infancy (PHHI). The main clinical characteristics of HI/HA syndrome are repeated episodes of symptomatic hypoglycemia, but not usually severe. Consequently, children with HI/HA syndrome are frequently not recognized in the first months of life. An 8-month-old boy was admitted to a hospital due to hypoglycemia seizures. He also had asymptomatic hyperammonemia with no signs of lethargy or headaches. Genetic testing revealed autosomal dominant syndrome, a mutation in the GLUD1 gene (p.Arg274Cys). The boy started treatment with diazoxide. Subsequent growth and neurological development were normal. Hypoglycemic symptoms in HI/HA syndrome may vary from being non specific to severe. As hypoglycemia could lead to brain injury and impairment of neurological development, timely diagnosis and management are essential. If transient hypoglycemia is ruled out, metabolic disorders must be taken into account.

Role of the allergist in diagnosis and management of patients with uveitis

JAMA ◽  
1966 ◽  
Vol 195 (3) ◽  
pp. 167-172 ◽  
Author(s):  
T. E. Van Metre
Keyword(s):  
Diagnosis And Management

The diagnosis and management of factor VIII and IX inhibitors: a guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO)

2000 ◽  
Vol 111 (1) ◽  
pp. 78-90 ◽  
Author(s):  
C. R. M. Hay ◽  
T. P. Baglin ◽  
P. W. Collins ◽  
F. G. H. Hill ◽  
D. M. Keeling
Keyword(s):  
Factor Viii ◽  
Diagnosis And Management ◽  
Viii And Ix ◽  
The Uk
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