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. 2016 Aug 8;37(10):1097–1105. doi: 10.1002/humu.23047

Table 1.

Clinical Laboratory Values for Affected Individuals with the Homozygous p.R142G FAH Variant

Proband Sister Brother Reference range
Blood
AFP 32,936 >40,000 41 <6 ng/ml
GGTP 14 18 9–24 U/l
AST 21 21 8–60 U/l
ALT 12 14 7–55 U/l
Bilirubin, Total, S 0.4 0.3 0.0–0.3 mg/dl
Bilirubin, Direct 0.1 0.1 0.0–0.3 mg/dl
PT 12.4 12 9.5–13.8 sec
APTT(S) 36 28–38 sec
INR 1 1 0.8–1.2
Tyrosine 55 106 31–106 nmol/ml
Phenylalanine 61 70 30–95 nmol/ml
Methionine 28 35 11–37 nmol/ml
ALA dehydratase 7.0 4.1 No reference range
Urine
5‐Aminolevulinic acid 16 25 ≤20 nmol/ml
Organic acids None detected None detected No reference range
Tyrosine 71 212 12–208 nmol/mg Cr
Methonine 8 18 <20 nmol/mg Cr
Phenylalanine 80 110 11–111 nmol/mg Cr

Clinical laboratory values for the proband, older deceased sister, and the affected younger brother. No abnormal urine organic acids (including succinylacetone, SUAC) were detected. Values in bold are outside the reference range.