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Chapter: 11 / Q: 11.27
All the following are recognized feature of Niemann-pick disease type B EXCEPT
Chapter: 11 / Q: 11.28
All the following lipidoses are inherited as an autosomal recessive traits EXCEPT
Chapter: 11 / Q: 11.29
Niemann-pick disease type A is characterized by all the following EXCEPT
Chapter: 11 / Q: 11.30
A 7-month-old boy presented with recurrent attacks of hypoglycemic seizures especially during an acute illness
Chapter: 11 / Q: 11.31
A 2-year-old girl presented with rapid deep breathing,hypoglycemia,recurrent epistaxis
Chapter: 11 / Q: 11.32
A 2-year-old boy presented with growth retardation, hepatomegaly, and recurrent attacks of hypoglycemical
Chapter: 11 / Q: 11.33
A 3-year-old girl presented with growth retardation,recurrent attacks of otitis media,
Chapter: 11 / Q: 11.34
The definitive diagnosis of type I glycogen storage disease GSD is by
Chapter: 11 / Q: 11.35
In von Gierke disease; treatment is designed to maintain normal blood glucose levels which is achieved by all the following EXCEPT
Chapter: 11 / Q: 11.36
A -9-month- old boy presented with persistent head lag, rapid breathing, difficult feeding, and hepatomegaly. Chest X- ray showed cardiomegaly
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