1.
Tunisie Medicale [La]. 2009; 87 (4): 295-296
in French
| IMEMR
| ID: emr-103077
Subject(s)
Humans , Male , Female , Facial Neoplasms , Head and Neck Neoplasms , Tomography, X-Ray Computed , Magnetic Resonance Imaging
2.
Tunisie Medicale [La]. 2008; 86 (9): 855-857
in French
| IMEMR
| ID: emr-90696
3.
Maghreb Medical. 2008; 28 (387): 34-36
in French
| IMEMR
| ID: emr-88652
ABSTRACT
Primary hyperoxaluria type I is an autosomal recessive disease due to congenital defect in alanine glyoxylate aminotransferase [ACT]. It is a rare disorder in witch only combined liver-kidney transplantation is curative. Our two cases of primary type I hyperoxaluria were particular by the early renal failure, thrombocytopenia and intestinal invagination. On the basis of our two cases we discuss diagnostic and therapeutic methods