Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters











Database
Type of study
Language
Publication year range
1.
J Pediatr ; 107(4): 537-41, 1985 Oct.
Article in English | MEDLINE | ID: mdl-4045602

ABSTRACT

Three brothers with diabetes mellitus, thiamine-responsive megaloblastic anemia, and sensorineural deafness are reported. Two had, in addition, congenital septal defects. The activities of thiamine-dependent enzymes were determined in one patient, revealing low alpha-ketoglutarate dehydrogenase activity, which could have caused a sideroblastic anemia with secondary megaloblastic changes. The anemia was thiamine dependent. The cause of the diabetes mellitus was not known, but it was not type 1.


Subject(s)
Anemia, Macrocytic/genetics , Anemia, Megaloblastic/genetics , Deafness/genetics , Diabetes Mellitus/genetics , Ketoglutarate Dehydrogenase Complex/deficiency , Ketone Oxidoreductases/deficiency , Thiamine/therapeutic use , Adolescent , Anemia, Megaloblastic/drug therapy , Child , Child, Preschool , Female , Genes, Recessive , Humans , Infant , Male , Pyruvate Dehydrogenase Complex/blood , Syndrome , Thiamine/administration & dosage , Transketolase/blood
SELECTION OF CITATIONS
SEARCH DETAIL