[CITATION][C] Glucoglycinuria, a new familial syndrome

H Käser, P Cottier, I Antener - The Journal of Pediatrics, 1962 - Elsevier
H Käser, P Cottier, I Antener
The Journal of Pediatrics, 1962Elsevier
A 9-year-old boy with cystic fibrosis of the pancreas was found to have also type B renal
glucosuria and hyperglycinuria without an increased excretion of other amino acids in the
urine. Investigation of 45 members of the patient's family revealed 13 apparently normal
relatives who also exhibited glucosuria and hyperglycinuria. The abnormality appears to be
transmitted as an autosomal dominant.
A 9-year-old boy with cystic fibrosis of the pancreas was found to have also type B renal glucosuria and hyperglycinuria without an increased excretion of other amino acids in the urine. Investigation of 45 members of the patient's family revealed 13 apparently normal relatives who also exhibited glucosuria and hyperglycinuria. The abnormality appears to be transmitted as an autosomal dominant.
Elsevier