Table 1 Biochemistry profile of the affected individuals
From: Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family
S. No. | Test | Patient VI-1 | Patient VI-3 |
|---|---|---|---|
| Â | Liver function | Â | Â |
1 | Serum bilirubin | 0.7 mg/dl | 0.9 mg/dl |
2 | Serum glutamate pyruvate transferase | 143 U/L | 135 U/L |
3 | Alkaline phosphatase | 911 U/L | 717 U/L |
| Â | Lipid profile | Â | Â |
4 | Triglyceride | 394 mg/dl | 406 mg/dl |
5 | Cholesterol | 155 mg/dl | 196 mg/dl |
6 | High density lipids | 14 mg/dl | 34 mg/dl |
7 | Low density lipids | 77 mg/dl | 129 mg/dl |
| Â | Serum electrolytes | Â | Â |
8 | Na+ | 141 | 144 |
9 | K+ | 3.71 | 3.99 |
10 | Cl- | 105.1 | 108.5 |
| Â | Sugar level | Â | Â |
11 | Fasting serum glucose | 124 mg/dl | 51 mg/dl |
12 | HbA1C | 6.5% | 5.6% |